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Bio1-C3-23-230

EUDAMED

Class IIa (EU MDR)

Ref 70100146591Model BIO1-C3-23-230

by FUJIFILM medwork GmbH

Identity

Trade Name
BIO1-C3-23-230 EUDAMED
Device Name
BIO1-Series EUDAMED
Model / Reference
BIO1-C3-23-230 EUDAMED
70100146591 EUDAMED

Identifiers

Primary DI / UDI-DI
04044503018212 EUDAMED
Basic UDI-DI
B-04044503018212 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-C3-23-230 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

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Manufacturer

EUDAMED SRN
DE-MF-000008444

Sources (1)

  • EUDAMED 26ef0ff6-8b9e-444e-93cb-2b082f570709 61 fields · synced Jul 23, 2026