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Gerber Sub-Acromion Retractor Left Modified

EUDAMED

Class I (EU MDR)

Ref 1641-02

by Innomed, Inc.

Identity

Trade Name
Gerber Sub-Acromion Retractor Left Modified EUDAMED
Device Name
Retractor EUDAMED
Model / Reference
1641-02 EUDAMED

Identifiers

Primary DI / UDI-DI
00840277101495 EUDAMED
Basic UDI-DI
8402771INNORETRACT016A EUDAMED
Direct Marketing DI
00840277101495 EUDAMED
EMDN Code
L0915 SPREADERS AND RETRACTORS FOR ORTHOPAEDIC SURGERY, REUSABLE 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

Gerber Sub-Acromion Retractor Left Modified by Innomed, Inc. — Class I — 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
Innomed, Inc.
EUDAMED SRN
US-MF-000014761
Authorised Representative
MediMark Europe Sarl. FR-AR-000000182

Sources (1)

  • EUDAMED 6ae62e11-8a1e-4f56-880c-c5e7a810aeff 61 fields · synced Jun 18, 2026