R2*/T2* Phantom v1.0
by Resonance Health Analysis Services Pty, Ltd.
R2*/T2* Phantom v1.0 is a Class I device made by Resonance Health Analysis Services Pty, Ltd., listed in FDA GUDID since 17 Apr 2024 (UDI-DI 09355529000088), 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 | Number09355529000088 | Date17 Apr 2024 | StatusListed |
Official records
- AccessGUDID record 09355529000088
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- R2*/T2* Phantom
- Generic name
- MRI phantom, test object
- Model / Ref / Catalog
- v1.0
- Primary DI / UDI-DI
- 09355529000088
- FDA product code
- IXG
- GMDN term
- MRI phantom, test object
- Device class
- Class I
- Regulation number
- 892.1950
- GUDID distribution status
- In Commercial Distribution
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