Probeat-V
by Hitachi High-Tech Corporation Japan GUDID
Product code LHN
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04560333350389 | Date1 Apr 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Recalls
-
- Terminated Z-1892-2019
There is a potential for a discrepant target position when using 3D3D matching mode in PIAS (Positioning Image Analysis System) software installed in the PROBEAT-V, proton therapy systems.
Specification
- Trade Name
- Probeat
- Generic Name
- Proton therapy system
- Model / Reference
- PROBEAT-V
- Primary DI / UDI-DI
- 04560333350389
- 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 7ad615e8-bf2e-4a20-acd5-18b2fcf02be8