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Podpätenka, silikón

EUDAMED

Class I (EU MDR)

Ref J 58365Model Insoles

by PROTETIKA, a.s.

Identity

Trade Name
Podpätenka, silikón EUDAMED
Model / Reference
Insoles EUDAMED
J 58365 EUDAMED

Identifiers

Primary DI / UDI-DI
08585003411968 EUDAMED
Basic UDI-DI
858500J58365SILPODM6V EUDAMED
Direct Marketing DI
08585003411968 EUDAMED
EMDN Code
Y061203 ORTHOSES, FOOT (INCLUDING INSOLES AND INSERTS) 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

Category: Orthotic insole, prefabricated, non-antimicrobial

Podpätenka, silikón by PROTETIKA, a.s. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Orthotic insole, prefabricated, non-antimicrobial.

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 b6cdd3a3-793a-40c4-a8e1-c76550b0fd92 61 fields · synced Jul 17, 2026