Skip to content

Disposable Biopsy Forceps

by Shangxian Minimal Invasive Inc. 14 variants

Ref SBF-A2323-2, SBF-B2323-2

Active European Union

CE MDD

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 26 Oct 2026. What this means

Regulatory status

as of registry sync 26 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDD NumberB-06970151100284 Basic UDI-DI Date7 Jun 2023RegisteredStatusActive

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

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDD Active

Specification

EUDAMED

Device Name
Disposable Biopsy Forceps
Model / Reference
SBF-A2323-2, SBF-B2323-2
Primary DI / UDI-DI
06970151100284, 06970151100291
Basic UDI-DI
B-06970151100284, B-06970151100291
EMDN Code
G0308010101 Gastrointestinal endoscopy, cold biopsy forceps, single-use
Device Class
Class IIa
EU market of registration
Norway

Manufacturer details

EUDAMED SRN
CN-MF-000018930
Authorised representative
MedPath GmbH DE-AR-000000087

Other devices from Shangxian Minimal Invasive Inc.

See all devices from Shangxian Minimal Invasive Inc. →

Properties

  • Implantable

Other properties (10)

  • Sterile: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No