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Gima

EUDAMED

Class IIa (EU MDR)

Ref 27008

by Razormed Inc.

Identity

Trade Name
GIMA EUDAMED
Device Name
Surgical Blades EUDAMED
Model / Reference
27008 EUDAMED

Identifiers

Primary DI / UDI-DI
18903376027666 EUDAMED
Basic UDI-DI
8903376SBWT EUDAMED
Unit of Use DI
08903376027669 EUDAMED
EMDN Code
V010301 BLADES WITH SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Gima by Razormed Inc. — 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

Manufacturer
Razormed Inc.
EUDAMED SRN
IN-MF-000012812
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 12f12314-6858-454a-999b-8944b0b31d77 61 fields · synced Jun 19, 2026