triton 09000
triton 09000 is a Class I device made by Core Labs, LLC, listed in FDA GUDID since 17 Nov 2017 (UDI-DI 00863897000351), registry data as of 8 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 | Number00863897000351 | Date17 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 00863897000351
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- triton
- Generic name
- X-ray system tube support, floor standing
- Model / Ref / Catalog
- 09000
- Primary DI / UDI-DI
- 00863897000351
- FDA product code
- IYB
- GMDN term
- X-ray system tube support, floor standing
- Device class
- Class I
- Regulation number
- 892.1770
- GUDID distribution status
- In Commercial Distribution
- MRI safety
- MR Unsafe
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