Chwilio Deddfwriaeth

Council Directive 2009/156/ECDangos y teitl llawn

Council Directive 2009/156/EC of 30 November 2009 on animal health conditions governing the movement and importation from third countries of equidae (codified version) (Text with EEA relevance)

Rhagor o Adnoddau

 Help about UK-EU Regulation

Legislation originating from the EU

When the UK left the EU, legislation.gov.uk published EU legislation that had been published by the EU up to IP completion day (31 December 2020 11.00 p.m.). On legislation.gov.uk, these items of legislation are kept up-to-date with any amendments made by the UK since then.

Close

Mae hon yn eitem o ddeddfwriaeth sy’n deillio o’r UE

Mae unrhyw newidiadau sydd wedi cael eu gwneud yn barod gan y tîm yn ymddangos yn y cynnwys a chyfeirir atynt gydag anodiadau.Ar ôl y diwrnod ymadael bydd tair fersiwn o’r ddeddfwriaeth yma i’w gwirio at ddibenion gwahanol. Y fersiwn legislation.gov.uk yw’r fersiwn sy’n weithredol yn y Deyrnas Unedig. Y Fersiwn UE sydd ar EUR-lex ar hyn o bryd yw’r fersiwn sy’n weithredol yn yr UE h.y. efallai y bydd arnoch angen y fersiwn hon os byddwch yn gweithredu busnes yn yr UE. EUR-Lex Y fersiwn yn yr archif ar y we yw’r fersiwn swyddogol o’r ddeddfwriaeth fel yr oedd ar y diwrnod ymadael cyn cael ei chyhoeddi ar legislation.gov.uk ac unrhyw newidiadau ac effeithiau a weithredwyd yn y Deyrnas Unedig wedyn. Mae’r archif ar y we hefyd yn cynnwys cyfraith achos a ffurfiau mewn ieithoedd eraill o EUR-Lex. The EU Exit Web Archive legislation_originated_from_EU_p3

Status:

EU Directives are published on this site to aid cross referencing from UK legislation. Since IP completion day (31 December 2020 11.00 p.m.) no amendments have been applied to this version.

  1. Introductory Text

  2. CHAPTER I GENERAL PROVISIONS

    1. Article 1.This Directive lays down animal health conditions for the movement...

    2. Article 2.For the purposes of this Directive the following definitions shall...

  3. CHAPTER II RULES FOR THE MOVEMENT OF EQUIDAE BETWEEN MEMBER STATES

    1. Article 3.Member States shall authorise the movement of registered equidae in...

    2. Article 4.(1) Equidae must show no clinical sign of disease at...

    3. Article 5.(1) A Member State which is not free from African...

    4. Article 6.Member States which implement an alternative control system providing guarantees...

    5. Article 7.(1) Equidae must be transported, as soon as possible, from...

    6. Article 8.(1) Member States shall ensure that: (a) registered equidae which...

    7. Article 9.The rules laid down in Directive 90/425/EEC shall apply in...

    8. Article 10.Veterinary experts from the Commission may, to the extent necessary...

  4. CHAPTER III RULES FOR IMPORTATION OF EQUIDAE FROM THIRD COUNTRIES

    1. Article 11.Equidae imported into the Community must satisfy the conditions laid...

    2. Article 12.(1) The importation of equidae into the Community shall only...

    3. Article 13.(1) The equidae must come from third countries which:

    4. Article 14.Before the day of loading for transportation to the Member...

    5. Article 15.Importation of equidae from the territory of a third country...

    6. Article 16.(1) The equidae must be identified in accordance with Article...

    7. Article 17.(1) Immediately upon arrival in the Member State of destination,...

    8. Article 18.Checks shall be carried out on the spot by veterinary...

    9. Article 19.In accordance with the procedure referred to in Article 21(2):...

  5. CHAPTER IV FINAL PROVISIONS

    1. Article 20.Annexes I to IV shall be amended in accordance with...

    2. Article 21.(1) The Commission shall be assisted by the Standing Committee...

    3. Article 22.Directive 90/426/EEC, as amended by the acts listed in Annex...

    4. Article 23.This Directive shall enter into force on the 20th day...

    5. Article 24.This Directive is addressed to the Member States.

  6. Signature

    1. ANNEX I

      COMPULSORILY NOTIFIABLE DISEASES

      1. The following diseases are compulsorily notifiable:

      2. Dourine Glanders Equine encephalomyelitis (of all types, including VEE) Infectious...

    2. ANNEX II

      1. MODEL HEALTH ATTESTATION

    3. ANNEX III

      1. MODEL HEALTH CERTIFICATE For trade between Member States EQUIDAE ANNEX IV...For trade between Member States EQUIDAE ANNEX IV AFRICAN HORSE...EQUIDAE ANNEX IV AFRICAN HORSE SICKNESS DIAGNOSIS Reagents for the...

    4. ANNEX IV

      1. AFRICAN HORSE SICKNESS DIAGNOSIS

        1. 1. COMPETITIVE ELISA FOR THE DETECTION OF ANTIBODIES TO AFRICAN HORSE...

          1. 1.1. Test procedure

            1. 1.1.1. Preparation of plates

              1. 1.1.1.1. Coat ELISA plates with AHSV antigen extracted from infected cell...

              2. 1.1.1.2. Wash plates three times by flooding and emptying the wells...

            2. 1.1.2. Control wells

              1. 1.1.2.1. Titrate the positive control sera in a twofold dilution series,...

              2. 1.1.2.2. Add 50 μl of the negative control serum at a...

              3. 1.1.2.3. Add 100 μl/well of blocking buffer to wells C and...

              4. 1.1.2.4. Add 50 μl of blocking buffer to wells E, F,...

            3. 1.1.3. Spot test method

              1. 1.1.3.1. Add a 1 in 5 dilution of each test serum...

            4. 1.1.4. Serum titration method

              1. 1.1.4.1. Prepare a twofold dilution series of each test sample (1...

            5. 1.1.5. Add 50 μl of guinea pig antisera, pre-diluted in blocking...

              1. 1.1.5.1. Incubate for 1 hour at 37 °C on an orbital shaker....

              2. 1.1.5.2. Wash plates three times and blot dry as before.

              3. 1.1.5.3. Add 50 μl of rabbit anti-guinea-pig horseradish peroxidase (HRP) conjugate...

              4. 1.1.5.4. Incubate for 1 hour at 37 °C on an orbital shaker....

              5. 1.1.5.5. Wash plates three times and blot dry as before.

            6. 1.1.6. Chromogen

            7. 1.1.7. Reading

          2. 1.2. Expression of results

            1. 1.2.1. Using a software package print out the optical density (OD)...

            2. 1.2.2. The diagnostic threshold (cut-off value) for test sera is 50 %...

        2. 2. INDIRECT ELISA FOR THE DETECTION OF ANTIBODIES TO AFRICAN HORSE...

          1. 2.1. Test procedure

            1. 2.1.1. Solid phase

              1. 2.1.1.1. ELISA plates are coated with recombinant AHSV-4 VP7 diluted in...

              2. 2.1.1.2. Wash the plates five times with distilled water containing 0,01 %...

              3. 2.1.1.3. Block the plates with phosphate buffered saline (PBS) + 5 %...

              4. 2.1.1.4. Remove the blocking solution and gently tap the plates onto...

            2. 2.1.2. Test samples

              1. 2.1.2.1. Serum samples to be tested, and positive and negative control...

              2. 2.1.2.2. Wash the plates as described in step 2.1.1.2.

            3. 2.1.3. Conjugate

              1. 2.1.3.1. Dispense 100 μl/well of horseradish-peroxidase (HRP) -conjugated anti-horse gamma-globulin diluted...

              2. 2.1.3.2. Wash the plates as described in step 2.1.1.2.

            4. 2.1.4. Cromogen/Substrate

              1. 2.1.4.1. Add 200 μl/well of chromogen/substrate solution (10 ml of 80,6...

              2. 2.1.4.2. Read the plates at 600 nm (or 620 nm).

          2. 2.2. Interpretation of the results

            1. 2.2.1. Calculate the cut-off value by adding 0,6 to the value...

            2. 2.2.2. Test samples giving absorbance values lower than the cut-off are...

            3. 2.2.3. Test samples giving absorbance values greater than the cut-off +...

            4. 2.2.4. Test samples giving intermediate absorbance values are doubtful and a...

        3. 3. BLOCKING ELISA FOR THE DETECTION OF ANTIBODIES TO AFRICAN HORSE...

          1. 3.1. Test procedure

            1. 3.1.1. ELISA plates

              1. 3.1.1.1. Coat ELISA plates with recombinant AHSV-4 VP7 diluted in carbonate/bicarbonate...

              2. 3.1.1.2. Wash the plates five times with phosphate buffered saline (PBS)...

              3. 3.1.1.3. Stabilise the plate by treatment with a stabilising solution (in...

            2. 3.1.2. Test samples and controls

            3. 3.1.3. Conjugate

            4. 3.1.4. Wash the plates five times with PBST and blot dry...

            5. 3.1.5. Chromogen/Substrate

            6. 3.1.6. Reading

          2. 3.2. Interpretation of the results

            1. 3.2.1. Assay validation

            2. 3.2.2. Cut-off calculation

            3. 3.2.3. Interpretation of results

    5. ANNEX V

      1. PART A

      2. PART B

    6. ANNEX VI

Yn ôl i’r brig

Options/Help

Print Options

Close

Mae deddfwriaeth ar gael mewn fersiynau gwahanol:

Y Diweddaraf sydd Ar Gael (diwygiedig):Y fersiwn ddiweddaraf sydd ar gael o’r ddeddfwriaeth yn cynnwys newidiadau a wnaed gan ddeddfwriaeth ddilynol ac wedi eu gweithredu gan ein tîm golygyddol. Gellir gweld y newidiadau nad ydym wedi eu gweithredu i’r testun eto yn yr ardal ‘Newidiadau i Ddeddfwriaeth’.

Gwreiddiol (Fel y’i mabwysiadwyd gan yr UE): Mae'r wreiddiol version of the legislation as it stood when it was first adopted in the EU. No changes have been applied to the text.

Pwynt Penodol mewn Amser: This becomes available after navigating to view revised legislation as it stood at a certain point in time via Advanced Features > Show Timeline of Changes or via a point in time advanced search.

Close

Dewisiadau Agor

Dewisiadau gwahanol i agor deddfwriaeth er mwyn gweld rhagor o gynnwys ar y sgrin ar yr un pryd

Close

Rhagor o Adnoddau

Gallwch wneud defnydd o ddogfennau atodol hanfodol a gwybodaeth ar gyfer yr eitem ddeddfwriaeth o’r tab hwn. Yn ddibynnol ar yr eitem ddeddfwriaeth sydd i’w gweld, gallai hyn gynnwys:

  • y PDF print gwreiddiol y fel adopted version that was used for the EU Official Journal
  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • pob fformat o’r holl ddogfennau cysylltiedig
  • slipiau cywiro
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill
Close

Llinell Amser Newidiadau

Mae’r llinell amser yma yn dangos y fersiynau gwahanol a gymerwyd o EUR-Lex yn ogystal ag unrhyw fersiynau dilynol a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig.

Cymerir dyddiadau fersiynau’r UE o ddyddiadau’r dogfennau ar EUR-Lex ac efallai na fyddant yn cyfateb â’r adeg pan ddaeth y newidiadau i rym ar gyfer y ddogfen.

Ar gyfer unrhyw fersiynau a grëwyd ar ôl y diwrnod ymadael o ganlyniad i newidiadau a wnaed gan ddeddfwriaeth y Deyrnas Unedig, bydd y dyddiad yn cyd-fynd â’r dyddiad cynharaf y daeth y newid (e.e. ychwanegiad, diddymiad neu gyfnewidiad) a weithredwyd i rym. Am ragor o wybodaeth gweler ein canllaw i ddeddfwriaeth ddiwygiedig ar Ddeall Deddfwriaeth.

Close

Rhagor o Adnoddau

Defnyddiwch y ddewislen hon i agor dogfennau hanfodol sy’n cyd-fynd â’r ddeddfwriaeth a gwybodaeth am yr eitem hon o ddeddfwriaeth. Gan ddibynnu ar yr eitem o ddeddfwriaeth sy’n cael ei gweld gall hyn gynnwys:

  • y PDF print gwreiddiol y fel adopted fersiwn a ddefnyddiwyd am y copi print
  • slipiau cywiro

liciwch ‘Gweld Mwy’ neu ddewis ‘Rhagor o Adnoddau’ am wybodaeth ychwanegol gan gynnwys

  • rhestr o newidiadau a wnaed gan a/neu yn effeithio ar yr eitem hon o ddeddfwriaeth
  • manylion rhoi grym a newid cyffredinol
  • pob fformat o’r holl ddogfennau cysylltiedig
  • dolenni i ddeddfwriaeth gysylltiedig ac adnoddau gwybodaeth eraill