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Medical Forceps and Clamps

by GRI Medical & Electronic Technology Co., Ltd. 7 variants

Ref 10-519006, 8603101, 8919020, AR-260175NS, 10-519003, 1306698, AR-30900NS

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number69319181F015KW Basic UDI-DI Date22 Jun 2023RegisteredStatusActive
United StatesGUDID listing GUDID Number16931918136660 UDI-DI Date11 Dec 2022ListedStatusListed GUDID: in commercial distribution

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

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  • Withdrawn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
B.braun
Generic Name
Dressing/utility forceps, scissors-like, single-use
Device Name
Medical Forceps and Clamps
Model / Reference
10-519006, 8603101, 8919020, AR-260175NS, 10-519003, 1306698, AR-30900NS
Primary DI / UDI-DI
16931918136660, 26931918197507, 16931918195254, 16931918109145, 16931918173122, 16931918125091, 16931918109329
Basic UDI-DI
69319181F015KW
FDA Product Code
GEN
EMDN Code
V9099 Various devices not included in other classes - other
GMDN Term
Dressing/utility forceps, scissors-like, single-use
Device Class
Class I
Regulation Number
878.4800
EU market of registration
Netherlands
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
SterileEUDAMED
No
Yes
GUDID
No

Manufacturer details

EUDAMED SRN
CN-MF-000004203
Authorised representative
Emergo Europe B.V. NL-AR-000000116

Related devices

Category: Device sterilization/disinfection container, reusable

Other devices from GRI Medical & Electronic Technology Co., Ltd.

See all devices from GRI Medical & Electronic Technology Co., Ltd. →

Properties

  • Sterile NoEUDAMEDGUDIDYesEUDAMED
  • Single Use
  • Premarket Exempt
  • Lot / Batch Number

Other properties (20)

  • 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
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No
  • Expiration Date: No
  • Manufacturing Date: No