UDI device identifier
Tatum Serrated Offset Surgical Curette 10S Serrated Offset Surgical Curette 10S
UDI device identifier 00083208131103 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208131103 |
|---|---|
| Brand name | Tatum Serrated Offset Surgical Curette 10S |
| Version or model | Serrated Offset Surgical Curette 10S |
| Catalog number | Curette Off/Serrated 10S |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | FZS |
| GMDN term | Bone curette, reusable |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 30, 2020 |
| Version date | Aug 25, 2021 |
| Description | Serrated Offset double ended Surgical Curette 10S |
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: