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0.9/1.2Screwdr.Bl., Cross, Self-Hold., 54mm

EUDAMED

Class I (EU MDR)

Ref M-2521

by Medartis AG

Identity

Trade Name
0.9/1.2Screwdr.Bl.,Cross,Self-Hold.,54mm EUDAMED
Device Name
Blades (not connected to an active device) EUDAMED
Model / Reference
M-2521 EUDAMED

Identifiers

Primary DI / UDI-DI
07630037874485 EUDAMED
Basic UDI-DI
76300378011P5 EUDAMED
EMDN Code
L99 SURGICAL INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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

0.9/1.2Screwdr.Bl., Cross, Self-Hold., 54mm by Medartis AG — 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
Medartis AG
EUDAMED SRN
CH-MF-000022291
Authorised Representative
Medartis GmbH DE-AR-000005810

Sources (1)

  • EUDAMED 4bdefe4a-c0c9-41ac-b517-2beda3ff413c 61 fields · synced Jul 23, 2026