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Captura Pro G47692

by Cook Incorporated

Ref BF-2.2S-230SP-20

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

CE MDR CE MDD

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 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED NumberB-00827002476929 Basic UDI-DI 00827002476929UDI-DIDate8 May 2026RegisteredStatusActive
European UnionCE/MDD EUDAMED NumberB-00827002476929 Basic UDI-DI 00827002476929UDI-DIDate8 May 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00827002476929 UDI-DI Date19 Mar 2018ListedStatusListed 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  • Withdrawn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, CE/MDD Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Captura Pro® EUDAMED
Captura Pro GUDID
Generic Name
Flexible endoscopic biopsy forceps, single-use
Device Name
Captura Pro Biopsy Forceps
Cold Biopsy Forceps
Model / Ref / Catalog
BF-2.2S-230SP-20, G47692
Primary DI / UDI-DI
00827002476929
Basic UDI-DI
B-00827002476929, 0827002WCM00000000023ML
FDA Product Code
PTS
EMDN Code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
GMDN Term
Flexible endoscopic biopsy forceps, single-use
Device Class
Class IIa EUDAMED
Class II GUDID
Regulation Number
876.1500
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
BF-2.2S-230SP-20
GUDID
G47692
Device ClassEUDAMED
Class IIa
GUDID
Class II

Related devices

Category: Flexible endoscopic biopsy forceps, single-use

Other devices from Cook Incorporated

See all devices from Cook Incorporated →

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