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Actical-Recertified

EUDAMED

Class IIa (EU MDR)

Ref U1081737

by Respironics Inc.

Identity

Trade Name
Actical-Recertified EUDAMED
Device Name
Actical EUDAMED
Model / Reference
U1081737 EUDAMED

Identifiers

Primary DI / UDI-DI
00606959409446 EUDAMED
Basic UDI-DI
B-00606959409446 EUDAMED
EMDN Code
Z12062599 KINEMATIC MOTION CAPTURE ANALYSIS SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Austria 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

Actical-Recertified by Respironics, Inc. — Class IIa — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Respironics Inc.
EUDAMED SRN
US-MF-000002301
Authorised Representative
Respironics Deutschland GmbH & Co.KG DE-AR-000006164

Sources (1)

  • EUDAMED 9e33988e-d280-4692-9a6b-a6c0b78e9abe 61 fields · synced Jun 18, 2026