Identity
- Trade Name
- Medi-First Cold Compress Large FDA UDI
- Generic Name
- Endothermic cold therapy pack FDA UDI
- Device Name
- A device intended to be applied with pressure to the body surface to provide cold therapy to help reduce fever, pain, and inflammation associated with joint/muscle/tissue injury and/or minor burns. FDA UDI
- Model / Reference
- 70201 FDA UDI
- Description
- A device intended to be applied with pressure to the body surface to provide cold therapy to help reduce fever, pain, and inflammation associated with joint/muscle/tissue injury and/or minor burns. FDA UDI
Identifiers
- Catalog Number
- 70201 FDA UDI
- Primary DI / UDI-DI
- 00347682702014 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
Yes
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Endothermic cold therapy pack
Medi-First Cold Compress Large by Medique Products — 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
- Medique Products
Sources (1)
- FDA UDI 68b7d4e2-c5a4-446a-9f04-3c61b783eb43 36 fields · synced May 30, 2026