← Back to catalogue

Bio1-G4-23-230

EUDAMED

Class IIa (EU MDR)

Ref 70100146557Model BIO1-G4-23-230

by FUJIFILM medwork GmbH

Identity

Trade Name
BIO1-G4-23-230 EUDAMED
Device Name
BIO1-Series EUDAMED
Model / Reference
BIO1-G4-23-230 EUDAMED
70100146557 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503024206 EUDAMED
Basic UDI-DI
B-04044503024206 EUDAMED
EMDN Code
G0308010101 GASTROINTESTINAL ENDOSCOPY, COLD BIOPSY FORCEPS, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Flexible endoscopic biopsy forceps, single-use

Bio1-G4-23-230 by FUJIFILM medwork GmbH — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Flexible endoscopic biopsy forceps, single-use.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
DE-MF-000008444

Sources (1)

  • EUDAMED 45d3e456-c62d-4dfa-ac03-2bbf475afbe9 61 fields · synced Jul 16, 2026