Varex Imaging ICX722B
Ref 167244
Varex Imaging ICX722B is an ionization chamber radiation measuring probe (EU MDD Class IIb; FDA Class I; FDA product code IZO, Generator, High-Voltage, X-Ray, Diagnostic) made by Varex Imaging Corporation, registered in EUDAMED on 19 May 2026 (Basic UDI-DI B-08718755003048) and listed in FDA GUDID since 4 Mar 2022 (UDI-DI 08718755003048), active as of 23 Oct 2026.
Active
CE MDD
Valid until
No date given
FDA recalls
Not checked
Documents
None linked in EUDAMED
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| European Union | CE/MDD EUDAMED | NumberB-08718755003048 08718755003048 | Date19 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number08718755003048 | Date4 Mar 2022 | StatusListed |
Official records
- EUDAMED public site B-08718755003048
- AccessGUDID record 08718755003048
Across registries
- EUDAMED Basic UDI-DI B-08718755003048 registered 19 May 2026 Active
- FDA GUDID UDI-DI 08718755003048 listed 4 Mar 2022 Listed
Timeline
- Listed FDA GUDID 08718755003048
- Registered EUDAMED B-08718755003048
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- Varex Imaging
- Generic name
- Ionization chamber radiation measuring probe
- Device name
- ICX722B
- Model / reference
- 167244 EUDAMEDICX722B GUDID
- Primary DI / UDI-DI
- 08718755003048
- Basic UDI-DI
- B-08718755003048
- FDA product code
- IZO
- EMDN code
- Z11030599 Radiology instruments - other
- GMDN term
- Ionization chamber radiation measuring probe
- Device class
- Class IIb EUDAMEDClass I GUDID
- Regulation number
- 892.1700
- EU registration type
- Legacy device (under a directive)
- EU market of registration
- Netherlands
- GUDID distribution status
- In Commercial Distribution
Truth per registry
| Field | EUDAMED | GUDID |
|---|---|---|
| Model / reference | 167244 | ICX722B |
| Device class | Class IIb | Class I |
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