UDI device identifier
TechLITE Pen Needle 4mm x 32g Sample 10's 234032
UDI device identifier 00015482230326 · Arkray USA, Inc.
Key facts
| Primary DI | 00015482230326 |
|---|---|
| Brand name | TechLITE Pen Needle 4mm x 32g Sample 10's |
| Version or model | 234032 |
| Company | Arkray USA, Inc. |
| DUNS number | 008171162 |
| Product code | FMI |
| GMDN term | Autoinjector needle |
| Premarket submission | K143437 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Feb 26, 2018 |
| Version date | Aug 24, 2026 |
| Description | Sterile Single-Use Pen Needle samples. Intended to be used with a pen injector device for the subcutaneous injection of insulin. |
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: