ThermaCare ColdWraps
by Pfizer Inc. GUDID
Withdrawn
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00305733040010 | Date29 May 2020 | StatusWithdrawn |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not known
- Not covered
United States — GUDID listing Listed
Recalls
No FDA recalls on record, checked 21 Oct 2026.
Specification
- Generic Name
- Exothermic heat therapy pack/patch
- Model / Reference
- ThermaCare ColdWraps
- Primary DI / UDI-DI
- 00305733040010
- FDA Product Code
- IMD
- GMDN Term
- Exothermic heat therapy pack/patch
- Device Class
- Class I
- Regulation Number
- 890.5710
- Commercial Distribution
- Not in Commercial Distribution
- MRI Safety
- MR Unsafe
Other devices from Pfizer Inc.
Properties
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