UDI device identifier
ARTOURA Breast Tissue Expander SMXP155RH
UDI device identifier 00081317024354 · MENTOR TEXAS L.P.
Key facts
| Primary DI | 00081317024354 |
|---|---|
| Brand name | ARTOURA Breast Tissue Expander |
| Version or model | SMXP155RH |
| Catalog number | SMXP155RH |
| Company | MENTOR TEXAS L.P. |
| DUNS number | 167450993 |
| Product code | LCJ |
| GMDN term | Skin-port tissue expander |
| Premarket submission | K161176 |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Jul 1, 2016 |
| Version date | Mar 31, 2026 |
| Description | Smooth, High Profile, Suture Tabs, Integral Injection Dome, 850cc |
At a glance
- 10–99 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: