Fuse 1.01
by Patterson Technology Center
Fuse 1.01 is a Class II device made by Patterson Technology Center, listed in FDA GUDID since 7 May 2018 (UDI-DI 00350227300019), registry data as of 23 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number00350227300019 | Date7 May 2018 | StatusListed |
Official records
- AccessGUDID record 00350227300019
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Fuse
- Generic name
- Radiological PACS-dedicated management software
- Model / reference
- 1.01
- Primary DI / UDI-DI
- 00350227300019
- FDA product code
- LLZ
- GMDN term
- Radiological PACS-dedicated management software
- Device class
- Class II
- Regulation number
- 892.2050
- GUDID distribution status
- In Commercial Distribution
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