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R&S

EUDAMED

Class IIa (EU MDR)

Ref 3151031

by Razormed Inc.

Identity

Trade Name
R&S EUDAMED
Device Name
Surgical Blades EUDAMED
Model / Reference
3151031 EUDAMED

Identifiers

Primary DI / UDI-DI
18903376036590 EUDAMED
Basic UDI-DI
8903376SBWT EUDAMED
Unit of Use DI
08903376036593 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
France 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

R&S 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 b8f31cb0-f1da-49fa-b400-ded9a13f9f69 61 fields · synced Jul 23, 2026