TBS iNsight 3.1.2
TBS iNsight 3.1.2 is a Class II device made by medimaps group SA, listed in FDA GUDID since 13 Jan 2022 (UDI-DI B214OSTBSI3120), 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 | NumberB214OSTBSI3120 | Date13 Jan 2022 | StatusListed |
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- TBS iNsight
- Generic name
- Bone absorptiometric x-ray system, dual-energy
- Model / reference
- 3.1.2
- Primary DI / UDI-DI
- B214OSTBSI3120
- FDA product code
- KGI
- GMDN term
- Bone absorptiometric x-ray system, dual-energy
- Device class
- Class II
- Regulation number
- 892.1170
- GUDID distribution status
- In Commercial Distribution
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