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Orteza

EUDAMED

Class I (EU MDR)

Ref P-5907739317827Model Orteza

by 4fizjo Group Sp. Z O. O.

Identity

Trade Name
ORTEZA EUDAMED
Device Name
Orteza EUDAMED
Model / Reference
Orteza EUDAMED
P-5907739317827 EUDAMED

Identifiers

Primary DI / UDI-DI
05907739317827 EUDAMED
Basic UDI-DI
590773931ORTEZAUT EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Poland 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: Ankle/foot orthosis

Orteza by 4fizjo Group Sp. Z O. O. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Ankle/foot orthosis.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PL-MF-000031702

Sources (1)

  • EUDAMED 61927c33-6542-40b7-97a9-23b54e371c0c 61 fields · synced Jun 18, 2026