6. CE marking of relevant devices that come within the scope of more than one Directive
10. Supplemental provisions relating to conformity assessment procedures
13. Designation of authorised representatives for registration purposes
AMENDMENTS TO THE 1994 REGULATIONS
1.In regulation 2(1) of the 1994 Regulations (interpretation)—
2.In regulation 3(2) of the 1994 Regulations (application of the...
3.After regulation 12 of the 1994 Regulations (general provisions relating...
4.In regulation 14 of the 1994 Regulations (registration of persons...
5.In regulation 16 of the 1994 Regulations (clinical investigations)—
6.In regulation 17 of the 1994 Regulations (notified bodies), after...
7.For paragraph (1) of regulation 18 of the 1994 Regulations...
9.After regulation 19 of the 1994 Regulations there shall be...
10.In paragraph (1) of regulation 22 of the 1994 Regulations...
11.In paragraph (1) of regulation 23 of the 1994 Regulations...