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Negus Artery Forceps Large

EUDAMED

Class I (EU MDR)

Ref G21-214Model Forceps - Reusable

by Sheffmed Limited

Identity

Trade Name
Negus Artery Forceps Large EUDAMED
Model / Reference
Forceps - Reusable EUDAMED
G21-214 EUDAMED

Identifiers

Primary DI / UDI-DI
05060417203772 EUDAMED
Basic UDI-DI
506041720FORCEP-RUWU EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Spain EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Category: Surgical retraction system, reusable

Negus Artery Forceps Large by Sheffmed Limited — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Surgical retraction system, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Sheffmed Limited
EUDAMED SRN
GB-MF-000004158
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 5584114c-f149-4b40-ae30-41a8a44275f6 61 fields · synced Aug 4, 2026