RadQual BM06V-20-33
by Radqual, LLC
Part of a family of 32 devices: see the family page
Ref BM06V-20-33
RadQual BM06V-20-33 is a Class I device made by Radqual, LLC, registered in EUDAMED on 7 May 2026 (Basic UDI-DI 0085002047CALIBRATIONUH) and listed in FDA GUDID since 3 Aug 2020 (UDI-DI 00850020470372), active as of 23 Oct 2026.
Active
CE MDR
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/MDR EUDAMED | Number0085002047CALIBRATIONUH 00850020470372 | Date7 May 2026 | StatusActive |
| United States | GUDID listing GUDID | Number00850020470372 | Date3 Aug 2020 | StatusListed |
Official records
- EUDAMED public site 0085002047CALIBRATIONUH
- AccessGUDID record 00850020470372
Across registries
- EUDAMED Basic UDI-DI 0085002047CALIBRATIONUH registered 7 May 2026 Active
- FDA GUDID UDI-DI 00850020470372 listed 3 Aug 2020 Listed
Timeline
- Listed FDA GUDID 00850020470372
- Registered EUDAMED 0085002047CALIBRATIONUH
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
- European Union
- United States
Specification
- Trade name
- RadQual
- Generic name
- Radionuclide source, quality assurance
- Device name
- Calibration Sources
- Model / reference
- BM06V-20-33
- Description
- Ba-133 20cc Multidose Vial
- Primary DI / UDI-DI
- 00850020470372
- Basic UDI-DI
- 0085002047CALIBRATIONUH
- FDA product code
- IXD
- EMDN code
- V9099 Various devices not included in other classes - other
- GMDN term
- Radionuclide source, quality assurance
- Device class
- Class I
- Regulation number
- 892.1400
- System or procedure pack
- System which is a device in itself
- EU registration type
- Standard device
- EU market of registration
- Austria
- GUDID distribution status
- In Commercial Distribution
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