UDI device identifier
LANZO Lancing Device 570015
UDI device identifier 00015482570156 · Arkray USA, Inc.
Key facts
| Primary DI | 00015482570156 |
|---|---|
| Brand name | LANZO Lancing Device |
| Version or model | 570015 |
| Company | Arkray USA, Inc. |
| DUNS number | 008171162 |
| Product code | FMK |
| GMDN term | Manual blood lancing device, reusable |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Oct 30, 2018 |
| Version date | Aug 24, 2026 |
| Description | A hand-held manual instrument intended to be used for controlled skin puncture to obtain a capillary blood specimen (e.g., performed by a diabetic patient) typically at the fingertip or ear lobe. It is used with a sterile, disposable lancet tip, and has a manually-powered mechanism (e.g… |
At a glance
- None MAUDE reports citing this UDI
- No 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: