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ThermaCare HeatWraps

by Pfizer Inc. 5 variants

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

Registry data, not yet checked by deviCERTS. Source GUDID, synced 1 Jun 2026. What this means

Regulatory status

as of registry sync 1 Jun 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00305733015971 UDI-DI Date29 May 2020ListedStatusListed 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  • Withdrawn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

Generic Name
Exothermic heat therapy pack/patch
Model / Reference
ThermaCare HeatWraps - Neck, Wrist & Shoulder
Primary DI / UDI-DI
00305733015971
FDA Product Code
IMD
GMDN Term
Exothermic heat therapy pack/patch
Device Class
Class I
Regulation Number
890.5710
GUDID distribution status
Not in Commercial Distribution
MRI Safety
MR Unsafe

Other devices from Pfizer Inc.

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Properties

  • Single Use
  • Over-the-Counter
  • Premarket Exempt
  • Lot / Batch Number
  • Expiration Date
  • Manufacturing Date

Other properties (8)

  • Sterile: No
  • Implantable: No
  • Contains Latex: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Serial Number: No