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Actiwatch Spectrum Device

EUDAMED

Class IIa (EU MDR)

Ref 1048091

by Respironics Inc.

Identity

Trade Name
Actiwatch Spectrum Device EUDAMED
Device Name
Actiwatch 2 and Actiwatch Spectrum EUDAMED
Model / Reference
1048091 EUDAMED

Identifiers

Primary DI / UDI-DI
00606959020535 EUDAMED
Basic UDI-DI
B-00606959020535 EUDAMED
EMDN Code
Z12040117 METABOLIC AND PHYSICAL ACTIVITY HOLTER SYSTEMS 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

Actiwatch Spectrum Device 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 b957ba75-3740-410e-855a-c3b3917faa86 61 fields · synced Jun 18, 2026