ORION System 1SOPT00023
by Bizlink Robotic Solutions France S.A.S. United States GUDID
Product code JAI
Regulatory status
Recall ongoing. 2 ongoing FDA recalls. See recalls
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number03700383510215 | Date10 Apr 2025 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Ongoing Z-0398-2024
- Ongoing Z-0399-2024
Users of the patient positioning system ORION System can be faced with a sudden short-term acceleration or with an unintended short-distance movement when the movements are again allowed after an unforeseen interruption signal of motion may result in a collision of the patient with another stationary component of the treatment room.
Specification
- Trade Name
- ORION System
- Generic Name
- Proton therapy system robotic patient positioner
- Model / Ref / Catalog
- 1SOPT00023
- Primary DI / UDI-DI
- 03700383510215
- 510(k) Number
- FDA Product Code
- JAI
- GMDN Term
- Proton therapy system robotic patient positioner
- Device Class
- Class II
- Regulation Number
- 892.5770
- Commercial Distribution
- In Commercial Distribution
Properties & raw data
Show properties, registry sources and raw records
Other properties (12)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Prescription Use: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
Sources (1)
- FDA UDI e4e57c81-3ba2-414b-b7db-deab1400bda7