Linde PRX-9632
Linde PRX-9632 is a Class I device made by Western Enterprises, Inc., listed in FDA GUDID since 12 Aug 2022 (UDI-DI B929PRX96320), 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 | NumberB929PRX96320 | Date12 Aug 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Linde
- Generic name
- Fixed medical gas cylinder regulator
- Model / Ref / Catalog
- PRX-9632
- Primary DI / UDI-DI
- B929PRX96320
- FDA product code
- CAN
- GMDN term
- Fixed medical gas cylinder regulator
- Device class
- Class I
- Regulation number
- 868.2700
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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