UDI device identifier
HYPO NDL 31GX1/2" HARD PACK 26391
UDI device identifier 00020221263916 · Exel International
Key facts
| Primary DI | 00020221263916 |
|---|---|
| Brand name | HYPO NDL 31GX1/2" HARD PACK |
| Version or model | 26391 |
| Catalog number | 26391 |
| Company | Exel International |
| DUNS number | 180572216 |
| Product code | FMF |
| GMDN term | Hypodermic needle, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Mar 15, 2023 |
| Version date | Jun 8, 2026 |
| Description | HYPO NDL 31GX1/2" HARD PACK, 100/BX 1000/CS TSK3113 |
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: