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Venus

EUDAMED

Class I (EU MDR)

Ref 1006010801

by HumanTech Spine GmbH

Identity

Trade Name
VENUS EUDAMED
Device Name
VN Handle EUDAMED
Model / Reference
1006010801 EUDAMED

Identifiers

Primary DI / UDI-DI
04250539932976 EUDAMED
Basic UDI-DI
42505399343NG 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

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: Surgical retraction system, reusable

Venus by HumanTech Spine GmbH — 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

EUDAMED SRN
DE-MF-000010596

Sources (1)

  • EUDAMED 93e116d2-0e2f-4622-adf2-d79b8ba72308 61 fields · synced Jun 14, 2026