UDI device identifier
MENTOR MemoryGel Xtra Resterilizable Gel Sizer RSZMPX160S
UDI device identifier 00081317025955 · MENTOR TEXAS L.P.
Key facts
| Primary DI | 00081317025955 |
|---|---|
| Brand name | MENTOR MemoryGel Xtra Resterilizable Gel Sizer |
| Version or model | RSZMPX160S |
| Catalog number | RSZ-MPX-160S |
| Company | MENTOR TEXAS L.P. |
| DUNS number | 167450993 |
| Product code | MRD |
| GMDN term | Invasive breast implant sizer, fixed, reusable |
| Premarket submission | K062421 |
| Device class | Unclassified |
| Single use | No |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Aug 31, 2017 |
| Version date | Mar 31, 2026 |
| Description | Moderate Plus Profile Xtra, M+X 160cc Gel Sizer |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ GUDID devices with this product code
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About UDI device identifiers (GUDID)
The Global Unique Device Identification Database (GUDID) holds the device identifiers (UDI-DIs) and key attributes that labelers submit to the FDA for devices that carry a unique device identifier.
Source: U.S. FDA Global Unique Device Identification Database (GUDID), via NLM AccessGUDID · Source date: