UDI device identifier
EXEL HYPO NDL 16GX1" BULK, NON-STERILIE; "NON SILICONIZED" 26421BNS
UDI device identifier 00020221464214 · Exel International
Key facts
| Primary DI | 00020221464214 |
|---|---|
| Brand name | EXEL HYPO NDL 16GX1" BULK, NON-STERILIE; "NON SILICONIZED" |
| Version or model | 26421BNS |
| Catalog number | 26421BNS |
| Company | Exel International |
| DUNS number | 180572216 |
| Product code | FMF |
| GMDN term | Hypodermic needle, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 6, 2023 |
| Version date | Jun 8, 2026 |
| Description | EXEL HYPO NDL 16GX1" BULK, NON-STERILIE; "NON SILICONIZED"; DOUBLE BAGGED, 5,000PCS/CASE, 20,000PCS/CARTON #777034019 BNNS |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- Yes 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: