UDI device identifier
Bruder Karpecki 99653
UDI device identifier 00041533996538 · The Hilsinger Company Parent, Llc
Key facts
| Primary DI | 00041533996538 |
|---|---|
| Brand name | Bruder Karpecki |
| Version or model | 99653 |
| Catalog number | 1094232 |
| Company | The Hilsinger Company Parent, Llc |
| DUNS number | 118449190 |
| Product code | HNA |
| GMDN term | Eye spud/needle |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 25, 2026 |
| Version date | Mar 5, 2026 |
| Description | KARPECKI DEBRIDER |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: