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BrownGuard 5000 ortéza hlezenní typ 01

EUDAMED

Class I (EU MDR)

Ref NAModel Ankle orthosis

by ARIES, a.s.

Identity

Trade Name
BrownGuard 5000 ortéza hlezenní typ 01 EUDAMED
Device Name
BrownGuard 5000 ankle orthosis type 01 EUDAMED
Model / Reference
Ankle orthosis EUDAMED
NA EUDAMED

Identifiers

Primary DI / UDI-DI
08590072961740 EUDAMED
Basic UDI-DI
85900722026043H EUDAMED
EMDN Code
Y06120601 PASSIVE ANKLE-FOOT ORTHOSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Czechia 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

BrownGuard 5000 ortéza hlezenní typ 01 by ARIES, a.s. — 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

Manufacturer
ARIES, a.s.
EUDAMED SRN
CZ-MF-000047385

Sources (1)

  • EUDAMED d0de6181-28ab-44b5-a980-a2ebf04732fc 61 fields · synced Jun 19, 2026