UDI device identifier
Accelerator III 4mm x 32cm Syringe Cannula III432-SYR
UDI device identifier 00081317021872 · MENTOR TEXAS L.P.
Key facts
| Primary DI | 00081317021872 |
|---|---|
| Brand name | Accelerator III 4mm x 32cm Syringe Cannula |
| Version or model | III432-SYR |
| Catalog number | III432-SYR |
| Company | MENTOR TEXAS L.P. |
| DUNS number | 167450993 |
| Product code | MUU |
| GMDN term | Liposuction system cannula, reusable |
| Premarket submission | K981172 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 23, 2016 |
| Version date | Mar 31, 2026 |
| Description | Accelerator III 4mm x 32cm Syringe Cannula |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: