UDI device identifier
SPLINTER OUT Splinter Out Kit - 28
UDI device identifier 00098108000039 · MediPoint Holdings LLC
Key facts
| Primary DI | 00098108000039 |
|---|---|
| Brand name | SPLINTER OUT |
| Version or model | Splinter Out Kit - 28 |
| Company | MediPoint Holdings LLC |
| DUNS number | 118797353 |
| Product code | LRR |
| GMDN term | First aid kit, medicated |
| Device class | Not classified |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 10, 2025 |
| Version date | Jul 18, 2025 |
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: