UDI device identifier
Tatum Surgical-Analog Analog ITI 6.0-8.0 XFer
UDI device identifier 00083208100611 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208100611 |
|---|---|
| Brand name | Tatum Surgical-Analog |
| Version or model | Analog ITI 6.0-8.0 XFer |
| Catalog number | Analog ITI 6.0-8.0 XFer |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | NDP |
| GMDN term | Dental implant suprastructure, temporary, preformed, single-use |
| Premarket submission | K811923 |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | Yes |
| Publish date | Feb 27, 2020 |
| Version date | Dec 9, 2020 |
| Description | Transfer Analog for ITI 6.0, 7.0 & 8.0mm Integrity Implants |
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: