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Neoprénová ortéza kolena KO-13

EUDAMED

Class I (EU MDR)

Ref J 74062Model Knee orthose

by PROTETIKA, a.s.

Identity

Trade Name
Neoprénová ortéza kolena KO-13 EUDAMED
Model / Reference
Knee orthose EUDAMED
J 74062 EUDAMED

Identifiers

Primary DI / UDI-DI
08585003409613 EUDAMED
Basic UDI-DI
858500J74062KO13MN6 EUDAMED
Direct Marketing DI
08585003409613 EUDAMED
EMDN Code
Y061209 KNEE ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Slovakia 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

Neoprénová ortéza kolena KO-13 by PROTETIKA, a.s. — 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
PROTETIKA, a.s.
EUDAMED SRN
SK-MF-000004489

Sources (1)

  • EUDAMED 66b1eb3a-23f1-4cae-9293-4ae5edbbc0bb 61 fields · synced Jun 18, 2026