UDI device identifier
ALLURA 3321-14-N
UDI device identifier 00065055100921 · PMT CORPORATION
Key facts
| Primary DI | 00065055100921 |
|---|---|
| Brand name | ALLURA |
| Version or model | 3321-14-N |
| Company | PMT CORPORATION |
| DUNS number | 039576871 |
| Product code | LCJ |
| GMDN term | Skin-port tissue expander |
| Premarket submission | K845036 |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Jun 28, 2021 |
| Version date | Jul 6, 2021 |
| Description | VAGINAL STENT, CYLINDRICAL, 4 SUTURE TABS, 4X14CM, 170CC FILL |
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: