UDI device identifier
Tatum Surgical Custom Abutment (Post) Custom Abutment
UDI device identifier 00083208700002 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208700002 |
|---|---|
| Brand name | Tatum Surgical Custom Abutment (Post) |
| Version or model | Custom Abutment |
| Catalog number | Custom PN 40° to 60° |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | NHA |
| GMDN term | Screw endosteal dental implant, two-piece |
| Premarket submission | K811923 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | Yes |
| Publish date | Jan 27, 2021 |
| Version date | May 27, 2021 |
| Description | Implant Abutment neck diameter ( 3.5 to 5.0mm), 9mm height, between 40° and 60° as required - prescribed for patient by Dentist |
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: