Osteo mat 03804536
Osteo mat 03804536 is a Class II device made by Siemens Healthcare GmbH, listed in FDA GUDID since 20 Jul 2018 (UDI-DI 04056869008837), registry data as of 12 Nov 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04056869008837 | Date20 Jul 2018 | StatusListed |
Official records
- AccessGUDID record 04056869008837
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Osteo mat
- Generic name
- Full-body CT system
- Model / reference
- 03804536
- Primary DI / UDI-DI
- 04056869008837
- FDA product code
- JAK
- GMDN term
- Full-body CT system
- Device class
- Class II
- Regulation number
- 892.1750
- GUDID distribution status
- In Commercial Distribution
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