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Hallustop

EUDAMED

Class I (EU MDR)

Ref DRIE0ALAXXULP

by mdh sp. z o. o.

Identity

Device Name
Hallustop EUDAMED
Model / Reference
DRIE0ALAXXULP EUDAMED

Identifiers

Primary DI / UDI-DI
05901780411398 EUDAMED
Basic UDI-DI
59017804DRIE0AJJ EUDAMED
Direct Marketing DI
05901780411398 EUDAMED
EMDN Code
Y061299 LOWER EXTREMITY ORTHOSES - OTHER 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

Hallustop by mdh sp. z o. o. — 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
mdh sp. z o. o.
EUDAMED SRN
PL-MF-000011406

Sources (1)

  • EUDAMED 2d05ebc5-e696-4f0f-be72-b609b92f9072 61 fields · synced Jun 18, 2026