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Actiwave Motion

by Camntech Limited

Actiwave Motion (08-565) is a Class II device made by Camntech Limited, listed in FDA GUDID since 24 Sep 2016 (UDI-DI B329AWVM33), not in commercial distribution (GUDID) as of 23 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing NumberB329AWVM33 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: not in commercial distribution

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Actiwave
Generic name
Kinesiology ambulatory recorder
Model / Ref / Catalog
Motion, 08-565
Primary DI / UDI-DI
B329AWVM33
FDA product code
LEL
GMDN term
Kinesiology ambulatory recorder
Device class
Class II
Regulation number
882.5050
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code LEL (Device, Sleep Assessment).

Other devices from Camntech Limited

  • Actiheart AH5

    Class II

  • Actiheart AH5 BT

    Class II

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)