Penlon Nuffield 200 MRI
by Penlon, Ltd.
Penlon Nuffield 200 MRI is a Class II device made by Penlon, Ltd., listed in FDA GUDID since 11 May 2016 (UDI-DI 05051977000086), 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 | Number05051977000086 | Date11 May 2016 | StatusListed |
Official records
- AccessGUDID record 05051977000086
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Penlon
- Generic name
- Portable pneumatic ventilator
- Model / reference
- Nuffield 200 MRI
- Primary DI / UDI-DI
- 05051977000086
- FDA product code
- BSZ
- GMDN term
- Portable pneumatic ventilator
- Device class
- Class II
- Regulation number
- 868.5160
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Conditional
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