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eyeMAX(TM) Single-Use Biopsy Forceps BF10004

by Micro-Tech (Nanjing) Co., Ltd.

Ref BF10004

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 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number6902284DF60378AF Basic UDI-DI 06902284575301UDI-DIDate2 Jul 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number06902284575301 UDI-DI Date28 Jun 2023ListedStatusListed 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  • Withdrawn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
eyeMAX(TM) Single-Use Biopsy Forceps
Generic Name
Flexible endoscopic biopsy forceps, single-use
Device Name
Single-Use SD Biopsy Forceps
Model / Reference
BF10004
Primary DI / UDI-DI
06902284575301 EUDAMED
46932503549408 GUDID
Basic UDI-DI
6902284DF60378AF
FDA Product Code
FCL
EMDN Code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class IIa EUDAMED
Class I GUDID
Regulation Number
876.1075
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution
Size
Length — 2300 Millimeter
Outer Diameter — 1.0 Millimeter

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Primary DI / UDI-DIEUDAMED
06902284575301
GUDID
46932503549408
Device ClassEUDAMED
Class IIa
GUDID
Class I

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Other devices from Micro-Tech (Nanjing) Co., Ltd.

See all devices from Micro-Tech (Nanjing) Co., Ltd. →

Properties

  • Sterile
  • Single Use
  • Prescription Use
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (17)

  • 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