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pocketCPR heartpush CPR-HTP-MW002

by HEART SAVER Inc.

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 23 Oct 2026. What this means

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number28800338830067 UDI-DI Date18 Aug 2026ListedStatusListed GUDID: 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  • Withdrawn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
pocketCPR heartpush
Generic Name
Cardiopulmonary resuscitation feedback device, manual
Model / Reference
CPR-HTP-MW002
Primary DI / UDI-DI
28800338830067
FDA Product Code
PMJ
GMDN Term
Cardiopulmonary resuscitation feedback device, manual
Device Class
Class II
Regulation Number
870.5210
GUDID distribution status
In Commercial Distribution

Other devices from HEART SAVER Inc.

Properties

  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Serial Number
  • Manufacturing Date

Other properties (9)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Expiration Date: No