Skip to content

Veni-Gard

by Conmed Corporation United States EUDAMEDGUDID

Ref 710-2730B, 730-4432

Product code KMKEMDN C010199

Regulatory status

as of 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD EUDAMED Number084585408540D9 Basic UDI-DIDate12 Nov 2025RegisteredStatusActive
European UnionCE/MDR EUDAMED Number084585408540D9 Basic UDI-DIDate12 Nov 2025RegisteredStatusActive
United StatesGUDID listing GUDID Number10653405014331 UDI-DIDate28 Apr 2020ListedStatusIn distribution

Coverage

2 jurisdictions

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Listed
  • Not covered
  • European Union CE/MDD, CE/MDR Active
  • United States GUDID listing Listed

Recalls: none on record (FDA, checked 22 Oct 2026)

Certificates: none listed in EUDAMED

Specification

EUDAMED · GUDID · synced 22 Oct 2026

Generic Name
Adhesive bandage
Vascular catheterization support/maintenance kit, non-medicated
Device Name
Non-orthopedic, Non-active, IV Stabilization, Non-sterile
Surgical Instruments and Accessories
Model / Ref / Catalog
710-2730B, 730-4432
Primary DI / UDI-DI
10653405014331, 10653405014423
Basic UDI-DI
084585408540D9, B-10653405014423
Unit of Use DI
00653405014334
FDA Product Code
KMK
EMDN Code
C010199 Peripheral i.v. catheters and cannulas - other
GMDN Term
Adhesive bandage
Vascular catheterization support/maintenance kit, non-medicated
Device Class
Class I
Regulation Number
880.5210
Market of Registration
Belgium
Commercial Distribution
In Commercial Distribution

Manufacturer details

EUDAMED SRN
US-MF-000012663
Authorised representative
MDSS GmbH DE-AR-000005430

Properties & raw data

Show properties, registry sources and raw records
  • Sterile NoEUDAMEDGUDIDYesEUDAMEDGUDID
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
Other properties (18)
  • Implantable: No
  • 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
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Manufacturing Date: No

Sources (4)

  • EUDAMED 44764dc8-c79b-4d12-9953-d057e9bd52d0 61 fields · synced 22 Oct 2026
  • FDA UDI 0e3c4394-bc7c-437c-8dcb-558f1fdf0b61 36 fields · synced 27 May 2026
  • FDA UDI 0231c96c-fc4f-4a6c-b915-82c8e855ea64 36 fields · synced 30 May 2026
  • EUDAMED 10653405014423|B-10653405014423 61 fields · synced 12 Jul 2026