Planmed Nuance Excel
by Planmed Oy
Planmed Nuance Excel is a Class II device made by Planmed Oy, listed in FDA GUDID since 8 Sep 2016 (UDI-DI 06430035430024), not in commercial distribution (GUDID) as of 22 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 | Number06430035430024 | Date8 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 06430035430024
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Trade name
- Planmed
- Generic name
- Stationary mammographic x-ray system, digital
- Model / reference
- Nuance Excel
- Primary DI / UDI-DI
- 06430035430024
- FDA product code
- MUE
- GMDN term
- Stationary mammographic x-ray system, digital
- Device class
- Class II
- Regulation number
- 892.1715
- GUDID distribution status
- Not in Commercial Distribution
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