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Single-use Grasping Forceps

EUDAMED

Class IIa (EU MDR)

Ref GFB-2318GModel GFA-(1806G,1812G,1818G,1823G),GFB-(2306G,2312G,2318G,2323G),GFC-(1806G,1812G,1818G,1823G,2306G,2312G,2318G,2323G)

by Scivita Medical Technology Co., Ltd.

Identity

Trade Name
Single-use Grasping Forceps EUDAMED
Device Name
Single-use Grasping Forceps EUDAMED
Model / Reference
GFA-(1806G,1812G,1818G,1823G),GFB-(2306G,2312G,2318G,2323G),GFC-(1806G,1812G,1818G,1823G,2306G,2312G,2318G,2323G) EUDAMED
GFB-2318G EUDAMED

Identifiers

Primary DI / UDI-DI
06971381258769 EUDAMED
Basic UDI-DI
697138125046A92 EUDAMED
Direct Marketing DI
06971381258769 EUDAMED
EMDN Code
U0903010101 COLD BIOPSY FORCEPS FOR UROGENITAL ENDOSCOPY, SINGLE-USE EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Single-use Grasping Forceps by Scivita Medical Technology Co., Ltd. — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000010305
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 3a2b9a61-d91a-4d23-a7e1-3b6923c6f636 61 fields · synced Jun 19, 2026