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Prolene

by Ethicon, LLC. EUDAMED

Active European Union

Ref 8725BGModel PROLENE Suture

Regulatory status

as of 28 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR NumberMDR 719658 Date5 Jun 2026IssuedStatusActive expires 4 Jul 2028

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  • Withdrawn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 719658 Supplemented

    Technical documentation EU MDR

    Notified body
    Notified body 2797
    Issued
    5 Jun 2026
    Expires
    4 Jul 2028
    Reason
    Other

Specification

EUDAMED

Device Name
PROLENE Suture
Model / Reference
PROLENE Suture, 8725BG
Primary DI / UDI-DI
10705031091610
Basic UDI-DI
0705031a012574X
EMDN Code
H010201010401,H010201010402
Device Class
Class III
Market of Registration
Belgium

Manufacturer details

EUDAMED SRN
US-MF-000013111
Authorised representative
Johnson & Johnson Medical GmbH DE-AR-000007712

Other devices from Ethicon Inc.

  • Coated VICRYL

    Class III
  • Prolene

    Class III
  • Perma-Hand

    Class III
  • Nurolon

    Class III
  • Mersilene

    Class III
  • Coated VICRYL

    Class III

See all devices from Ethicon Inc. →

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