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Coated VICRYL VCP947H

by Ethicon Inc.

Ref VCP947HModel Vicryl Plus Antibacterial

Active European Union. Also listed in GUDID (US), not in commercial distribution.

CE MDR

Valid until

7 Mar 2028

CE MDR certificate

FDA recalls

None found

in data synced 24 Oct 2026

Documents

1 certificate

Certifier BSI Group The Netherlands B.V.

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberMDR 730033 Date28 Jul 2026IssuedStatusActive expires 7 Mar 2028
United StatesGUDID listing GUDID Number10705031079786 UDI-DI Date29 May 2017ListedStatusListed GUDID: not in commercial distribution

Certificates

1 certificate · EUDAMED

EUDAMED certificates (1)
  • MDR 730033 Active Supplemented

    Technical documentation EU MDR

    Certifier
    BSI Group The Netherlands B.V. 2797
    Issued
    28 Jul 2026
    Expires
    7 Mar 2028
    Reason
    Other

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 24 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
VICRYL Plus EUDAMED
Coated VICRYL GUDID
Generic Name
Polyester suture, bioabsorbable, multifilament, antimicrobial
Device Name
Vicryl Plus Antibacterial Polyglactin 910 Braided Absorbable Suture
Model / Ref / Catalog
VCP947H, Vicryl Plus Antibacterial
Primary DI / UDI-DI
10705031079786
Basic UDI-DI
0705031a007925K
510(k) Number
FDA Product Code
GAM
EMDN Code
H010101040201 Polyglycolic acid with lactic acid with antibacterial multifilament with needle
GMDN Term
Polyester suture, bioabsorbable, multifilament, antimicrobial
Device Class
Class III EUDAMED
Class II GUDID
Regulation Number
878.4493
EU market of registration
Belgium
GUDID distribution status
Not in Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class III
GUDID
Class II

Related devices

Cleared under the same submission (K132580)

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Properties

  • Sterile
  • Single Use
  • Implantable
  • Incorporates Medicinal Product
  • Prescription Use
  • Combination Product
  • Lot / Batch Number
  • Expiration Date

Other properties (16)

  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No