aries 04000
aries 04000 is a Class II device made by Core Labs, LLC, listed in FDA GUDID since 17 Nov 2017 (UDI-DI 00863897000320), 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 | Number00863897000320 | Date17 Nov 2017 | StatusListed |
Official records
- AccessGUDID record 00863897000320
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- aries
- Generic name
- Basic diagnostic x-ray system table, powered
- Model / Ref / Catalog
- 04000
- Primary DI / UDI-DI
- 00863897000320
- FDA product code
- IXQ
- GMDN term
- Basic diagnostic x-ray system table, powered
- Device class
- Class II
- Regulation number
- 892.1980
- GUDID distribution status
- In Commercial Distribution
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