ARCADIS Orbic 10143407
ARCADIS Orbic 10143407 is a Class II device made by Siemens Healthcare GmbH, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 04056869009025), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04056869009025 | Date24 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04056869009025
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- ARCADIS Orbic
- Generic name
- Portable general-purpose fluoroscopic x-ray system, analogue
- Model / reference
- 10143407
- Primary DI / UDI-DI
- 04056869009025
- FDA product code
- OXO
- GMDN term
- Portable general-purpose fluoroscopic x-ray system, analogue
- Device class
- Class II
- Regulation number
- 892.1650
- GUDID distribution status
- In Commercial Distribution
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