UDI device identifier
TopCare Insulin Syringe 102912
UDI device identifier 00036800250789 · Topco Associates, LLC
Key facts
| Primary DI | 00036800250789 |
|---|---|
| Brand name | TopCare Insulin Syringe |
| Version or model | 102912 |
| Company | Topco Associates, LLC |
| DUNS number | 072943876 |
| Product code | FMF |
| GMDN term | Insulin syringe/needle, basic |
| Premarket submission | K062702 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 4, 2016 |
| Version date | Dec 31, 2025 |
| Description | 1cc 12.7mm 29G Insulin Syringe, Sterile, Single-Use, 100ct |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: