PART VF92Notified BodiesF92Approved Bodies, Conformity Assessment Bodies and Marking of Products
F16Interpretation of Part V44A
In this Part, “medical device” means a device that is a “relevant device” for the purposes of Part II, III or IV.
F71Meaning of approved body and UK notified bodyA45
1
An approved body is a conformity assessment body which—
a
has been designated by the Secretary of State pursuant to the procedure set out in regulation 45 (designation etc. of approved bodies); or
b
immediately before IP completion day was a UK notified body in respect of which the Secretary of State has taken no action under regulation 45(5) to withdraw a designation.
2
In this regulation—
“UK notified body” means a body which the Secretary of State had before IP completion day notified to the European Commission in accordance with Article 3(7) of Commission Implementing Regulation (EU) 920/2013 or under Article 15 of Directive 98/79.”.
Designation etc. of F103approved bodiesE645
1
The Secretary of State may designate for the purposes of F52these Regulations any corporate or other body as a body which is to carry out any of the tasks of F9an approved body, and, if he so designates a body (referred to in these Regulations as F88an “approved body”), he shall designate the tasks which it is to carry out.
2
A body may be designated under paragraph (1) as a body which is to carry out tasks of F26an approved body only if—
a
b
c
d
in so far as it needs to be able to fulfil the functions of an importing Party arising out of F61a mutual recognition agreement, it is able to do so.
3
The Secretary of State may refuse to designate a body under paragraph (1) if it fails to pay any fee payable under Part VI in connection with an application for designation.
4
The Secretary of State may vary the tasks that F62an approved body may carry out, and if he does, those varied tasks will be the tasks which it is designated to carry out.
5
The Secretary of State may place a restriction in relation to, or withdraw, any designation of a body under paragraph (1) if—
a
the body so requests;
b
he considers that it is no longer a body in respect of which the applicable criteria for designation set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F76both read with Regulation (EU) No 722/2012 or Annex IX of Directive 98/79 are met; or
c
he considers that the body is not capable of fulfilling the functions of an importing Party arising out of F39a mutual recognition agreement which it needs to be able to fulfil,
and the Secretary of State may also withdraw any designation of a body under paragraph (1) if it fails to pay any fee payable under Part VI.
6
Before—
a
effecting a variation under paragraph (4); or
b
restricting or withdrawing a designation under paragraph (5),
7
For the purpose of deciding whether or not a body is one in respect of which the criteria set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F87both read with Regulation (EU) No 722/2012 or Annex IX of Directive 98/79 are met as respects the tasks which the body wants to carry out, or carries out, or for the purposes of deciding whether or not a body is capable of fulfilling the functions of an importing Party arising out of F8a mutual recognition agreement which it needs to be able to fulfil, the Secretary of State may arrange for the inspection of—
a
any premises occupied, or plant or equipment used, in connection with the carrying out of any such task; or
b
any premises occupied, or plant or equipment used, by a manufacturer where the body is undertaking any task in relation to that manufacturer,
and may take into account for the purposes of his decision the results of any such inspection and any refusal to afford him such facilities or assistance as he may reasonably require in order to carry out any such inspection.
8
The Secretary of State may request that F37an approved body supply to him any or all relevant information and documents, including budgetary documents, necessary—
a
to enable him to verify that the body meets the criteria set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F42both read with Regulation (EU) No 722/2012, or Annex IX of Directive 98/79; or
b
for the purposes of deciding whether or not the body is capable of fulfilling the functions of an importing Party arising out of F98a mutual recognition agreement which it needs to be able to fulfil,
and the body shall supply to him any and all relevant information or documents so requested.
Designation etc. of UK notified bodiesE245
1
The Secretary of State may designate for the purposes of article 11 of Directive 90/385, article 16 of Directive 93/42 or article 15 of Directive 98/79 any corporate or other body as a body which is to carry out any of the tasks of a notified body F14with respect to devices to be placed on the market in Northern Ireland, and, if he so designates a body (referred to in these Regulations as a “UK notified body”), he shall designate the tasks which it is to carry out.
2
A body may be designated under paragraph (1) as a body which is to carry out tasks of a notified body only if—
a
in so far as it is to be designated as a body which is to carry out tasks included in Directive 90/385, it is a body in respect of which the criteria for the designation of notified bodies set out in Annex 8 of that Directive F113, read with Regulation (EU) No 722/2012, are met;
b
c
in so far as it is to be designated as a body which is to carry out tasks included in Directive 98/79, it is a body in respect of which the criteria for the designation of notified bodies set out in Annex IX of that Directive are met; and
d
in so far as it needs to be able to fulfil the functions of an importing Party arising out of the Mutual Recognition Agreements, it is able to do so.
3
The Secretary of State may refuse to designate a body under paragraph (1) if it fails to pay any fee payable under Part VI in connection with an application for designation.
4
The Secretary of State may vary the tasks that a UK notified body may carry out, and if he does, those varied tasks will be the tasks which it is designated to carry out.
5
The Secretary of State may place a restriction in relation to, or withdraw, any designation of a body under paragraph (1) if—
a
the body so requests;
b
he considers that it is no longer a body in respect of which the applicable criteria for designation set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F116both read with Regulation (EU) No 722/2012 or Annex IX of Directive 98/79 are met; or
c
he considers that the body is not capable of fulfilling the functions of an importing Party arising out of the Mutual Recognition Agreements which it needs to be able to fulfil,
and the Secretary of State may also withdraw any designation of a body under paragraph (1) if it fails to pay any fee payable under Part VI.
6
Before—
a
effecting a variation under paragraph (4); or
b
restricting or withdrawing a designation under paragraph (5),
otherwise than at the notified body’s request, the Secretary of State shall give to the notified body an opportunity to make representations to him in writing and shall take into account any such representations as are made.
7
For the purpose of deciding whether or not a body is one in respect of which the criteria set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F112both read with Regulation (EU) No 722/2012 or Annex IX of Directive 98/79 are met as respects the tasks which the body wants to carry out, or carries out, or for the purposes of deciding whether or not a body is capable of fulfilling the functions of an importing Party arising out of the Mutual Recognition Agreements which it needs to be able to fulfil, the Secretary of State may arrange for the inspection of—
a
any premises occupied, or plant or equipment used, in connection with the carrying out of any such task; or
b
any premises occupied, or plant or equipment used, by a manufacturer where the body is undertaking any task in relation to that manufacturer,
and may take into account for the purposes of his decision the results of any such inspection and any refusal to afford him such facilities or assistance as he may reasonably require in order to carry out any such inspection.
8
The Secretary of State may request that a UK notified body supply to him any or all relevant information and documents, including budgetary documents, necessary—
a
to enable him to verify that the body meets the criteria set out in Annex 8 of Directive 90/385, Annex XI of Directive 93/42, F115both read with Regulation (EU) No 722/2012, or Annex IX of Directive 98/79; or
b
for the purposes of deciding whether or not the body is capable of fulfilling the functions of an importing Party arising out of the Mutual Recognition Agreements which it needs to be able to fulfil,
and the body shall supply to him any and all relevant information or documents so requested.
F80Choice of approved bodies and conformity assessment bodiesE346
Where a conformity assessment procedure involves the intervention of F33an approved body, including work which may be carried out by a third country conformity assessment body, the manufacturer of a device or F23the manufacturer’s UK responsible person may apply to F45any approved body or third country conformity assessment body to carry out tasks under that procedure which are within the framework of tasks which the body is designated to carry out.
Choice of notified bodies and conformity assessment bodiesE1446
Where a conformity assessment procedure involves the intervention of a notified body, including work which may be carried out by a third country conformity assessment body, the manufacturer of a device or his authorised representative may apply to any notified body or third country conformity assessment body to carry out tasks under that procedure which are within the framework of tasks which the body is designated to carry out.
F40General matters relating to approved bodiesE1047
1
F109An approved body to which an application has been made by a manufacturer or F108the manufacturer’s UK responsible person to perform the functions of F5an approved body under a conformity assessment procedure set out in F2these Regulations shall perform those functions, in accordance with the requirements of the procedure, if those functions are within the framework of tasks which the body is designated to carry out.
2
Where a manufacturer or F25the manufacturer’s UK responsible person has supplied information or data to F19an approved body in the course of a conformity assessment procedure, that body may, where duly justified, require the manufacturer to provide any additional information or data which it considers necessary for the purposes of that procedure.
3
4
F4An approved body shall, as respects a medical device which it has assessed F86..., inform all F79other approved bodies and the Secretary of State of—
a
all certificates suspended or withdrawn; and
b
on request, all certificates issued or refused,
and shall also make available to them, on request, any or all additional relevant information.
5
a
the applicable requirements of F64these Regulations have not been met or are no longer met; or
b
a certificate issued by it should not have been issued,
it may (having regard in particular to the principle of proportionality and the ability of the manufacturer to take appropriate corrective measures) suspend or withdraw the certificate issued in respect of that device or place restrictions on it, and in such cases, or in cases where the F77approved body is aware of circumstances in which the Secretary of State may need to take action pursuant to regulation 61, the F77approved body shall inform the Secretary of State thereof.
6
The Secretary of State may request that F38an approved body supply to him any information and documents that the Secretary of State may, having regard to the terms of F93a mutual recognition agreement, need to supply to a Party to F93a mutual recognition agreement, and the body shall supply to him any and all information or documents so requested.
8
F689
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F6810
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
General matters relating to UK notified bodiesE947
1
A UK notified body to which an application has been made by a manufacturer or his authorised representative to perform the functions of a notified body under a conformity assessment procedure set out in the Medical Devices Directives shall perform those functions, in accordance with the requirements of the procedure, if those functions are within the framework of tasks which the body is designated to carry out.
2
Where a manufacturer or his authorised representative has supplied information or data to a UK notified body in the course of a conformity assessment procedure, that body may, where duly justified, require the manufacturer to provide any additional information or data which it considers necessary for the purposes of that procedure.
3
The information, data and correspondence that a manufacturer or his authorised representative supplies to a notified body in the course of a conformity assessment procedure set out in the Medical Devices Directives shall, if the notified body is within the United Kingdom, be in English or some other Community language acceptable to the notified body concerned.
4
A UK notified body shall, as respects a medical device which it has assessed F111..., inform all other notified bodies and the Secretary of State of—
a
all certificates suspended or withdrawn; and
b
on request, all certificates issued or refused,
and shall also make available to them, on request, any or all additional relevant information.
5
Where a UK notified body finds, as respects a medical device which it has assessed F111..., that—
a
the applicable requirements of the Medical Devices Directives have not been met or are no longer met; or
b
a certificate issued by it should not have been issued,
it may (having regard in particular to the principle of proportionality and the ability of the manufacturer to take appropriate corrective measures) suspend or withdraw the certificate issued in respect of that device or place restrictions on it, and in such cases, or in cases where the notified body is aware of circumstances in which the Secretary of State may need to take action pursuant to regulation 61, the notified body shall inform the Secretary of State thereof.
6
The Secretary of State may request that a UK notified body supply to him any information and documents that the Secretary of State may, having regard to the terms of the Mutual Recognition Agreements, need to supply to a Party to the Mutual Recognition Agreements, and the body shall supply to him any and all information or documents so requested.
8
A UK notified body shall provide conformity assessment bodies with all the information it is required to provide to those bodies under the Mutual Recognition Agreements.
F1149
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F11410
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
F29Register of approved bodiesE847A
1
The Secretary of State must ensure that—
a
each approved body is assigned an identification number; and
b
there is a register of—
i
approved bodies;
ii
their approved body identification number;
iii
the tasks for which they have been designated; and
iv
any restrictions on those tasks.
2
The Secretary of State must ensure that the register referred to in paragraph (1) is maintained and made publicly available.
3
The Secretary of State may authorise the United Kingdom Accreditation Service to compile and maintain the register in accordance with paragraph (1)(b).
F57Register of UK notified bodiesE447A
1
The Secretary of State must ensure that—
a
each notified body established in the United Kingdom is assigned an identification number; and
b
there is a register of—
i
notified bodies established in the United Kingdom;
ii
their notified body identification number;
iii
the tasks for which they have been notified;
iv
any restrictions on those tasks.
2
The Secretary of State must ensure that the register referred to in paragraph (1) is maintained and made publicly available.
3
The Secretary of State may authorise the United Kingdom Accreditation Service to compile and maintain the register in accordance with paragraph (1)(b).
Designation etc. of F75... conformity assessment bodiesE1548
1
The Secretary of State may designate for the purposes of F48a mutual recognition agreement any corporate or other body as a body which is to carry out any of the tasks of a F30... conformity assessment body, and, if he so designates a body (referred to in these Regulations as F91a “CAB”), he shall designate the tasks which it is to carry out.
2
3
The Secretary of State may refuse to designate a body under paragraph (1) if it fails to pay any fee payable under Part VI in connection with an application for designation.
4
The Secretary of State may vary the tasks that F83a CAB may carry out, and if he does, those varied tasks will be the tasks which it is designated to carry out.
5
The Secretary of State may place a restriction in relation to, or withdraw, any designation of a body under paragraph (1) if—
a
the body so requests; or
b
and the Secretary of State may also withdraw any designation of a body under paragraph (1) if it fails to pay any fee payable under Part VI.
6
Before—
a
effecting a variation under paragraph (4); or
b
restricting or withdrawing a designation under paragraph (5),
7
For the purpose of deciding whether or not a body is capable of fulfilling the functions of F63a CAB arising out of F36a mutual recognition agreement which it needs to be able to fulfil, the Secretary of State may arrange for the inspection of—
a
any premises occupied, or plant or equipment used, in connection with the carrying out of any such task; or
b
any premises occupied, or plant or equipment used, by a manufacturer where the body is undertaking any task in relation to that manufacturer,
and may take into account for the purposes of his decision the results of any such inspection and any refusal to afford him such facilities or assistance as he may reasonably require in order to carry out any such inspection.
8
The Secretary of State may request that F15a CAB supply to him any or all relevant information and documents, including budgetary documents, necessary for the purposes of deciding whether or not the body is capable of fulfilling the functions of F15a CAB arising out of F67a mutual recognition agreement which it needs to be able to fulfil, and the body shall supply to him any and all relevant information or documents so requested.
Designation etc. of F105... conformity assessment bodiesE1148
1
The Secretary of State may designate for the purposes of F44a UK mutual recognition agreement any corporate or other body as a body which is to carry out any of the tasks of a F24... conformity assessment body, and, if he so designates a body (referred to in these Regulations as F47a “CAB”), he shall designate the tasks which it is to carry out.
2
3
The Secretary of State may refuse to designate a body under paragraph (1) if it fails to pay any fee payable under Part VI in connection with an application for designation.
4
The Secretary of State may vary the tasks that F49a CAB may carry out, and if he does, those varied tasks will be the tasks which it is designated to carry out.
5
The Secretary of State may place a restriction in relation to, or withdraw, any designation of a body under paragraph (1) if—
a
the body so requests; or
b
and the Secretary of State may also withdraw any designation of a body under paragraph (1) if it fails to pay any fee payable under Part VI.
6
Before—
a
effecting a variation under paragraph (4); or
b
restricting or withdrawing a designation under paragraph (5),
7
For the purpose of deciding whether or not a body is capable of fulfilling the functions of F94a CAB arising out of F84a UK mutual recognition agreement which it needs to be able to fulfil, the Secretary of State may arrange for the inspection of—
a
any premises occupied, or plant or equipment used, in connection with the carrying out of any such task; or
b
any premises occupied, or plant or equipment used, by a manufacturer where the body is undertaking any task in relation to that manufacturer,
and may take into account for the purposes of his decision the results of any such inspection and any refusal to afford him such facilities or assistance as he may reasonably require in order to carry out any such inspection.
8
The Secretary of State may request that F96a CAB supply to him any or all relevant information and documents, including budgetary documents, necessary for the purposes of deciding whether or not the body is capable of fulfilling the functions of F96a CAB arising out of F106a UK mutual recognition agreement which it needs to be able to fulfil, and the body shall supply to him any and all relevant information or documents so requested.
F54Fees charged by approved bodies and conformity assessment bodiesE549
1
F97An approved body or CAB may charge a fee in accordance with paragraphs (2), (3) and (4) for anything done in, or in connection with—
F34a
in the case of an approved body, performing the functions of an approved body or an importing Party under these Regulations or a mutual recognition agreement; and
2
Except as provided for by paragraph (3), the fee charged in respect of anything done shall not exceed an amount which reasonably represents the cost incurred, or to be incurred, in doing it.
3
Where the F85approved body or CAB charging the fee is a body the activities of which are carried on for profit, the fee may include an amount representing a profit which is reasonable in the circumstances, having regard to—
a
the character and extent of the work done or to be done by the F10approved body; and
b
the commercial rate normally charged in respect of profit for that work or similar work.
4
The F7approved body or CAB may require payment of the fee, or a reasonable estimate of the fee, in advance of carrying out the work in respect of which the fee is payable and as a condition of doing that work.
F51Fees charged by UK notified bodies and conformity assessment bodiesE1249
1
A UK notified body or F72CAB may charge a fee in accordance with paragraphs (2), (3) and (4) for anything done in, or in connection with—
a
in the case of a UK notified body, performing the functions of a notified body or an importing Party under F50the Medical Devices Directives or a UK mutual recognition agreement in respect of a conformity assessment procedure set out in the Medical Devices Directives or these Regulations as they apply in Great Britain; and
2
Except as provided for by paragraph (3), the fee charged in respect of anything done shall not exceed an amount which reasonably represents the cost incurred, or to be incurred, in doing it.
3
Where the UK notified body or F100CAB charging the fee is a body the activities of which are carried on for profit, the fee may include an amount representing a profit which is reasonable in the circumstances, having regard to—
a
the character and extent of the work done or to be done by the notified body; and
b
the commercial rate normally charged in respect of profit for that work or similar work.
4
The UK notified body or F11CAB may require payment of the fee, or a reasonable estimate of the fee, in advance of carrying out the work in respect of which the fee is payable and as a condition of doing that work.
Products incorrectly marked with F90an approved body or conformity assessment body numberE1350
1
No person shall—
a
affix F55an approved body or conformity assessment body number to a medical device if that body has not carried out an assessment in respect of that device for that person;
b
supply a medical device (if that supply is also a placing on the market, or if that supply is of a device which has been placed on the market) which has affixed to it F55an approved body or conformity assessment body number if that body—
i
has not carried out an assessment in respect of that device, or has not carried out that assessment for the person responsible for placing the device on the market, or
ii
has had its designation as F55an approved body or conformity assessment body withdrawn.
2
No person shall provide information comprising F82an approved body or conformity assessment body number on a medical device, the instructions for use for a medical device, or the sales packaging for a medical device if that device—
a
is being or has been placed on the market; and
b
F56the approved body or conformity assessment body—
i
has not carried out an assessment in respect of that device, or has not carried out that assessment for the person responsible for placing the device on the market, or
ii
has had its designation as F82an approved body or conformity assessment body withdrawn.
3
Where the sectoral annex on medical devices in a Mutual Recognition Agreement under which a conformity assessment body was designated states that the annex does not apply to devices of a particular class or description, no person may supply a medical device of that class or description bearing the number of that conformity assessment body (if that supply is also a placing on the market or putting into service or is of a device that has been placed on the market or put into service) unless—
a
an assessment has been carried out on that device for the person responsible for placing it on the market or putting it into service by F6an approved body; and
4
For the purposes of this regulation, F27an approved body shall be taken to have carried out an assessment in respect of a device if it has endorsed a report prepared by a third country conformity assessment body in respect of that device.
Products incorrectly marked with a notified body or conformity assessment body numberE150
1
No person shall—
a
affix a notified body or conformity assessment body number to a medical device if that body has not carried out an assessment in respect of that device for that person;
b
supply a medical device (if that supply is also a placing on the market, or if that supply is of a device which has been placed on the market) which has affixed to it a notified body or conformity assessment body number if that body—
i
has not carried out an assessment in respect of that device, or has not carried out that assessment for the person responsible for placing the device on the market, or
ii
has had its designation as a notified body or conformity assessment body withdrawn.
2
No person shall provide information comprising a notified body or conformity assessment body number on a medical device, the instructions for use for a medical device, or the sales packaging for a medical device if that device—
a
is being or has been placed on the market; and
b
the notified body or conformity assessment body—
i
has not carried out an assessment in respect of that device, or has not carried out that assessment for the person responsible for placing the device on the market, or
ii
has had its designation as a notified body or conformity assessment body withdrawn.
3
Where the sectoral annex on medical devices in a Mutual Recognition Agreement under which a conformity assessment body was designated states that the annex does not apply to devices of a particular class or description, no person may supply a medical device of that class or description bearing the number of that conformity assessment body (if that supply is also a placing on the market or putting into service or is of a device that has been placed on the market or put into service) unless—
a
an assessment has been carried out on that device for the person responsible for placing it on the market or putting it into service by a notified body; and
b
the device bears the notified body number of that notified body.
4
For the purposes of this regulation, a notified body shall be taken to have carried out an assessment in respect of a device if it has endorsed a report prepared by a third country conformity assessment body in respect of that device.
Products incorrectly marked with a F17UK markingE1651
1
No person shall—
a
affix the F104UK marking for a medical device to a product which is not a medical device; or
b
supply a product (if that supply is also a placing on the market, or if that supply is of a product which has been placed on the market) which has affixed to it the F104UK marking for a medical device if that product is not a medical device.
2
No person shall provide information comprising a F104UK marking for a medical device on a product, the instructions for use for a product, or the sales packaging for a product if the product is not a medical device.
Products incorrectly marked with a CE markingE751
1
No person shall—
a
affix the CE marking for a medical device to a product which is not a medical device; or
b
supply a product (if that supply is also a placing on the market, or if that supply is of a product which has been placed on the market) which has affixed to it the CE marking for a medical device if that product is not a medical device.
2
No person shall provide information comprising a CE marking for a medical device on a product, the instructions for use for a product, or the sales packaging for a product if the product is not a medical device.
Words in Pt. 5 heading substituted (E.W.S.) (31.12.2020) by The Medical Devices (Amendment etc.) (EU Exit) Regulations 2019 (S.I. 2019/791), regs. 1(1), 7(2) (as amended by S.I. 2020/1478, reg. 1(3), Sch. 2 paras. 2, 47); 2020 c. 1, Sch. 5 para. 1(1)