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Absolok Extra

by Johnson & Johnson Medical GmbH EUDAMED

Active European Union

Ref AP202Model Absolok

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number0705031a0063654 Basic UDI-DIDate23 Dec 2025RegisteredStatusActive

Coverage

1 jurisdiction

SwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered

European Union — CE/MDR Active

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 735690 Amended

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    17 Oct 2024
    Expires
    9 Nov 2027
    Reason
    Other

Specification

EUDAMED

Device Name
Absorbable ligature clips
Model / Reference
Absolok, AP202
Primary DI / UDI-DI
10705031135482
Basic UDI-DI
0705031a0063654
EMDN Code
H03030102 Single absorbable clips for hemostasis in open and video surgery
Device Class
Class III
Market of Registration
Germany

Manufacturer details

EUDAMED SRN
DE-MF-000007714

Other devices from Johnson & Johnson Medical GmbH

See all devices from Johnson & Johnson Medical GmbH →

Properties

  • Sterile
  • Implantable

Other properties (11)

  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No