Green GuardInstant Cold Pack 3302
by Greenguard
Green GuardInstant Cold Pack 3302 is a Class I device made by Greenguard, listed in FDA GUDID since 26 Jun 2019 (UDI-DI 00347682033026), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00347682033026 | Date26 Jun 2019 | StatusListed |
Official records
- AccessGUDID record 00347682033026
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Green GuardInstant Cold Pack
- Generic name
- Endothermic cold therapy pack
- Model / Ref / Catalog
- 3302
- Primary DI / UDI-DI
- 00347682033026
- FDA product code
- IMD
- GMDN term
- Endothermic cold therapy pack
- Device class
- Class I
- Regulation number
- 890.5710
- GUDID distribution status
- In Commercial Distribution
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