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Actiwave 2E

by Camntech Limited

Actiwave 2E (08-521) is a Class II device made by Camntech Limited, listed in FDA GUDID since 24 Sep 2016 (UDI-DI B329AWV02E25), 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 NumberB329AWV02E25 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  • Withdrawn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
Telemetric electrocardiographic ambulatory recorder
Model / Ref / Catalog
2E, 08-521
Primary DI / UDI-DI
B329AWV02E25
FDA product code
MWJ
GMDN term
Telemetric electrocardiographic ambulatory recorder
Device class
Class II
Regulation number
870.2800
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code MWJ (Electrocardiograph,Ambulatory(Without Analysis)).

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)