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Spinal surgery spongiosa pushers

EUDAMED

Class I (EU MDR)

Ref 892201501Model 10000230814

by Richard Wolf GmbH

Identity

Device Name
Spinal surgery spongiosa pushers EUDAMED
Model / Reference
10000230814 EUDAMED
892201501 EUDAMED

Identifiers

Primary DI / UDI-DI
04055207068335 EUDAMED
Basic UDI-DI
405520706022019-0018176EU EUDAMED
Direct Marketing DI
04055207068335 EUDAMED
EMDN Code
Z12021199 ORTHOPAEDIC ENDOSCOPY INSTRUMENTS - 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: Rigid endoscope obturator

Spinal surgery spongiosa pushers by Richard Wolf GmbH — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Rigid endoscope obturator.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Richard Wolf GmbH
EUDAMED SRN
DE-MF-000007048

Sources (1)

  • EUDAMED e78aaa88-85cd-42ba-b8d6-9ebb78f4710f 61 fields · synced Jul 9, 2026