UDI device identifier
TechLITE® Lancets, 28g 880128
UDI device identifier 00015482880187 · Arkray USA, Inc.
Key facts
| Primary DI | 00015482880187 |
|---|---|
| Brand name | TechLITE® Lancets, 28g |
| Version or model | 880128 |
| Company | Arkray USA, Inc. |
| DUNS number | 008171162 |
| Product code | QRL |
| GMDN term | Blood lancing device tip |
| Premarket submission | K220475 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2018 |
| Version date | Aug 24, 2026 |
| Description | TechLITE Lancets 28g 100's. The lancet is intended for capillary blood sampling. |
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: