UDI device identifier
3ML LATEX-FREE LDS GASKET, BULK NON-STERILE 26201DG
UDI device identifier 00020221062014 · Exel International
Key facts
| Primary DI | 00020221062014 |
|---|---|
| Brand name | 3ML LATEX-FREE LDS GASKET, BULK NON-STERILE |
| Version or model | 26201DG |
| Catalog number | 26201DG |
| Company | Exel International |
| DUNS number | 180572216 |
| Product code | FMF |
| GMDN term | General-purpose syringe, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 5, 2023 |
| Version date | Oct 7, 2025 |
| Description | 3ML LATEX-FREE LDS GASKET, BULK NON-STERILE; 20,000PC/CRTN |
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: