Xe-102V
Xe-102V is a xenon administration system (FDA Class II; FDA product code CBP, Valve, Non-Rebreathing) made by Medi Nuclear Corp., Inc., listed in FDA GUDID since 9 Nov 2020 (UDI-DI 00850022357220), 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 | Number00850022357220 | Date9 Nov 2020 | StatusListed |
Official records
- AccessGUDID record 00850022357220
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Xenon administration system, diagnostic x-ray/CT
- Model / reference
- XE-102V
- Primary DI / UDI-DI
- 00850022357220
- FDA product code
- CBP
- GMDN term
- Xenon administration system, diagnostic x-ray/CT
- Device class
- Class II
- Regulation number
- 868.5870
- GUDID distribution status
- In Commercial Distribution
Similar devices
Other devices filed under FDA product code CBP (Valve, Non-Rebreathing).
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- CPR Face Mask by Genuine First Aid, LLC
- CPR BIO-BARRIER FACESHEILD by O-Two Systems Intl., Inc.
- Non-Rebreathing T Piece by Dhd Medical Products Div. Diemolding Corp.
- Lifeguard Vent Mask by Breath of Life, Inc.
- CPR MICROMASK PLUS CATALOG NO 73-402 by Plasco, Inc.
- ONE-WAY VALVE (WITH CONNECTOR) by Instrumentation Industries, Inc.
- NON-REBREATHING 'T' (BE 117) by Instrumentation Industries, Inc.