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ActiPatch 088

by Bioelectronics Corporation 10 variants

ActiPatch 088 (720-4) is a Class II device made by Bioelectronics Corporation, listed in FDA GUDID since 23 Jul 2020 (UDI-DI 00851329005340), registry data as of 2 Nov 2026.

Listed FDA GUDID listing, no authorization on record

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 2 Nov 2026.

Regulatory status

as of registry sync 2 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00851329005340 UDI-DI Date23 Jul 2020ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — GUDID listing Listed

Specification

GUDID

Trade name
ActiPatch
Generic name
Hand-held deep-tissue electromagnetic stimulator
Model / Ref / Catalog
088, 720-4
Primary DI / UDI-DI
00851329005340
FDA product code
PQY
GMDN term
Hand-held deep-tissue electromagnetic stimulator
Device class
Class II
Regulation number
890.5290
GUDID distribution status
In Commercial Distribution

Other devices from Bioelectronics Corporation

See all devices from Bioelectronics Corporation →

Properties

  • Over-the-counter
  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)