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Actiwatch 2

FDA UDI

Class II (US FDA UDI)

by Respironics, Inc.

Identity

Trade Name
Actiwatch 2 FDA UDI
Generic Name
Kinesiology ambulatory recorder FDA UDI
Device Name
Actiwatch 2 Dock Sub Assembly FDA UDI
Model / Reference
Actiwatch 2 Dock Sub Assembly FDA UDI
Description
Actiwatch 2 Dock Sub Assembly FDA UDI

Identifiers

Catalog Number
1047045 FDA UDI
Primary DI / UDI-DI
00606959043862 FDA UDI
FDA Product Code
GWQ FDA UDI
GMDN Term
Kinesiology ambulatory recorder FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Kinesiology ambulatory recorder

Actiwatch 2 by Respironics, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Kinesiology ambulatory recorder.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Respironics, Inc.

Sources (1)

  • FDA UDI 2467f38d-50f3-4c2b-8312-f93bc2684903 36 fields · synced Jun 1, 2026