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Neoprénová bandáž lakťa

EUDAMED

Class I (EU MDR)

Ref J 22122Model Elbow orthoseRef 8585003408098

by PROTETIKA, a.s.

Identity

Trade Name
Neoprénová bandáž lakťa EUDAMED
Neoprénová bandáž lakťa, LA-1 EUDAMED
Model / Reference
Elbow orthose EUDAMED
J 22122 EUDAMED
8585003408098 EUDAMED

Identifiers

Primary DI / UDI-DI
08585003408098 EUDAMED
Basic UDI-DI
858500J22122LA1XSST7 EUDAMED
Direct Marketing DI
08585003408098 EUDAMED
EMDN Code
Y060615 ELBOW 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 bandáž lakťa 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 (2)

  • EUDAMED 90a59267-8ea3-4dcf-b40c-8e2d0aee5ccf 61 fields · synced Jun 18, 2026
  • EUDAMED 020c6e1e-13c4-400d-aa5b-3bc8f856a027 61 fields · synced Jun 18, 2026