Identity
- Trade Name
- Green Guard Instant Cold Pack 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 - large FDA UDI
- Model / Reference
- 3300 FDA UDI
- Description
- A device intended to be applied with pressure to the body surface to provide cold therapy - large FDA UDI
Identifiers
- Catalog Number
- 3300 FDA UDI
- Primary DI / UDI-DI
- 00347682033002 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
Green Guard Instant Cold Pack by Greenguard — 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
- Greenguard
Sources (1)
- FDA UDI 35cb9b89-397e-4cf8-9c34-6abd9aa4f2cc 36 fields · synced May 31, 2026