Fuse 1.06
by Patterson Technology Center
Fuse 1.06 is a Class II device made by Patterson Technology Center, listed in FDA GUDID since 9 Nov 2019 (UDI-DI 00350227300040), 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 | Number00350227300040 | Date9 Nov 2019 | StatusListed |
Official records
- AccessGUDID record 00350227300040
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- Withdrawn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
- 1.06
- Primary DI / UDI-DI
- 00350227300040
- 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
Similar devices in this category
Other devices filed under Radiological PACS software.
- McKesson Radiology 12.3 by Change Healthcare Canada Company
- INFINITT Cardiology PACS by INFINITT Healthcare Co., Ltd.
- Change Healthcare Radiology Solutions 14.0 by Change Healthcare Canada Company
- INFINITT RT PACS by INFINITT Healthcare Co., Ltd.
- Visage Ease Pro 2.2 by Visage Imaging, Inc.
- Vitrea Software Package VSTP-002A by CANON INC.
- Sidexis 4 6773258 by SIRONA Dental Systems GmbH
- ContourProtégéAI - CT Thorax 1.0 by MIM SOFTWARE INC.