MobileDaRt Evolution 503-79888-41
MobileDaRt Evolution 503-79888-41 is a Class II device made by Shimadzu Corporation, listed in FDA GUDID since 10 Nov 2016 (UDI-DI 04540217053506), 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 | Number04540217053506 | Date10 Nov 2016 | StatusListed |
Official records
- AccessGUDID record 04540217053506
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- MobileDaRt Evolution
- Generic name
- Mobile basic diagnostic x-ray system, digital
- Model / reference
- 503-79888-41
- Primary DI / UDI-DI
- 04540217053506
- FDA product code
- IZL
- GMDN term
- Mobile basic diagnostic x-ray system, digital
- Device class
- Class II
- Regulation number
- 892.1720
- GUDID distribution status
- In Commercial Distribution
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