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Razormed

EUDAMED

Class I (EU MDR)

Ref 02999

by Razormed Inc.

Identity

Trade Name
RAZORMED EUDAMED
Device Name
STITCH CUTTERS EUDAMED
Model / Reference
02999 EUDAMED

Identifiers

Primary DI / UDI-DI
18903376029998 EUDAMED
Basic UDI-DI
8903376SCWV EUDAMED
EMDN Code
V0199 CUTTING DEVICES, SINGLE-USE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

Category: Cranial bur, single-use

Razormed by Razormed Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Cranial bur, single-use.

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 bd09fa0c-7a19-4cb4-a188-5f474c7b40b0 61 fields · synced Jun 19, 2026