Decompression of Choice E9022-e
Decompression of Choice E9022-e is a Class II device made by Pivotal Health Solutions, listed in FDA GUDID since 11 Aug 2022 (UDI-DI 00850020142392), 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 | Number00850020142392 | Date11 Aug 2022 | StatusListed |
Official records
- AccessGUDID record 00850020142392
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Decompression of Choice
- Generic name
- Programmable powered traction system
- Model / reference
- E9022-e
- Primary DI / UDI-DI
- 00850020142392
- FDA product code
- ITH
- GMDN term
- Programmable powered traction system
- Device class
- Class II
- Regulation number
- 890.5900
- GUDID distribution status
- In Commercial Distribution
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