UDI device identifier
Actuvate Splinter Out 98108199078 ACT
UDI device identifier 00098108000022 · MediPoint Holdings LLC
Key facts
| Primary DI | 00098108000022 |
|---|---|
| Brand name | Actuvate Splinter Out |
| Version or model | 98108199078 ACT |
| Company | MediPoint Holdings LLC |
| DUNS number | 118797353 |
| Product code | HTF |
| GMDN term | Dermal curette, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 29, 2023 |
| Version date | Nov 25, 2024 |
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: