Probeat
by Hitachi High-Tech Corporation Japan GUDID
Product code LHN
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04560333350358 | Date1 Apr 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-1838-2015
At a PROBEAT III site installed in Japan, the operator of the system found that the radiation was delivered inconsistent with the treatment plan and stopped the irradiation. The irradiation control system may be potentially affected when rebooting a part of the control system.
Specification
- Generic Name
- Proton therapy system
- Model / Reference
- PROBEAT WITH DISCRETE SPOT SCANNING SYSTEM
- Primary DI / UDI-DI
- 04560333350358
- 510(k) Number
- FDA Product Code
- LHN
- GMDN Term
- Proton therapy system
- Device Class
- Class II
- Regulation Number
- 892.5050
- Commercial Distribution
- In Commercial Distribution
Other devices from Hitachi High-Tech Corporation
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: 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 dbb4072a-4df4-462e-881a-eee656981eb3