Serenys Dr
by Metaltronica SpA Italy GUDID
Product code MUE
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number08052405210203 | Date25 May 2026 | StatusIn distribution |
Coverage
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic Name
- Stationary mammographic x-ray system, digital
- Model / Ref / Catalog
- SERENYS DR, M-DGM10/2D
- Primary DI / UDI-DI
- 08052405210203
- 510(k) Number
- FDA Product Code
- MUE
- GMDN Term
- Stationary mammographic x-ray system, digital
- Device Class
- Class II
- Regulation Number
- 892.1715
- Commercial Distribution
- In Commercial Distribution
Other devices from Metaltronica SpA
Properties & raw data
Show properties, registry sources and raw records
Other properties (11)
- Sterile: No
- Single Use: No
- Implantable: No
- Contains Latex: No
- Over-the-Counter: No
- Convenience Kit: No
- Combination Product: No
- HCT/P: No
- Premarket Exempt: No
- Lot / Batch Number: No
- Expiration Date: No
Sources (1)
- FDA UDI 95649bbc-8a75-4482-9d92-1870f2d03152