Identity
- Trade Name
- PARENT'S CHOICE FDA UDI
- Generic Name
- Endothermic cold therapy pack FDA UDI
- Device Name
- Perineal Cold Pack FDA UDI
- Model / Reference
- WALPCP-001 FDA UDI
- Description
- Perineal Cold Pack FDA UDI
Identifiers
- Primary DI / UDI-DI
- 00194346231454 FDA UDI
- FDA Product Code
- IMD FDA UDI
- GMDN Term
- Endothermic cold therapy pack FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 890.5710 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endothermic cold therapy pack
Parent's Choice by Walmart Stores — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class I | Pending data |
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Manufacturer
- Manufacturer
- Walmart Stores
Sources (1)
- FDA UDI d82efb42-11e7-4dea-a9e9-0f5de7561134 33 fields · synced May 30, 2026