Squid Rx Wrist
Squid Rx Wrist is a Class I device made by Portable Therapeutix, listed in FDA GUDID since 21 Jul 2023 (UDI-DI 00811107020866), registry data as of 22 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 | Number00811107020866 | Date21 Jul 2023 | StatusListed |
Official records
- AccessGUDID record 00811107020866
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Squid Rx
- Generic name
- Inflatable hot/cold therapy pack/electric pump
- Model / reference
- Wrist
- Primary DI / UDI-DI
- 00811107020866
- FDA product code
- IME, IRP
- GMDN term
- Inflatable hot/cold therapy pack/electric pump
- Device class
- Class I
- Regulation number
- 890.5700, 890.5650
- GUDID distribution status
- In Commercial Distribution
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