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Venus

EUDAMED

Class IIb (EU MDR)

Ref 4000025525-S

by HumanTech Spine GmbH

Identity

Trade Name
VENUS EUDAMED
Device Name
VE Screw S R EUDAMED
Model / Reference
4000025525-S EUDAMED

Identifiers

Primary DI / UDI-DI
04250539926432 EUDAMED
Basic UDI-DI
42505399406NF EUDAMED
EMDN Code
P09070302 THORACOLUMBOSACRAL FIXATION SYSTEMS EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Sutures

Yes

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

Venus by HumanTech Spine GmbH — Class IIb — 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

EUDAMED SRN
DE-MF-000010596

Sources (1)

  • EUDAMED 96d38d21-5d6c-4917-8b39-b4544d85a66c 61 fields · synced Sep 30, 2026