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CMS - Rotary peg, 5

EUDAMED

Class III (EU MDR)

Ref 341603

by BEZNOSKA, s.r.o.

Identity

Trade Name
CMS - Rotary peg, 5 EUDAMED
Device Name
KNEE REPLACEMENT SYSTEMS AND ANCILLARY ELEMENTS FOR KNEE REPLACEMENT EUDAMED
Model / Reference
341603 EUDAMED

Identifiers

Primary DI / UDI-DI
08592602123079 EUDAMED
Basic UDI-DI
859260202001EW EUDAMED
EMDN Code
P09098002 KNEE PROSTHESES ADAPTERS (INCLUDING CONES AND SLEEVES) EUDAMED

Classification

Device Class
Class III EUDAMED
Market of Registration
Czechia EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

Yes

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: Knee arthroplasty wedge

CMS - Rotary peg, 5 by BEZNOSKA, s.r.o. — Class III — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Knee arthroplasty wedge.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
BEZNOSKA, s.r.o.
EUDAMED SRN
CZ-MF-000000543

Sources (1)

  • EUDAMED e25dc542-2921-419c-8834-65cacee59b04 61 fields · synced Jul 19, 2026