UDI device identifier
DDP Retractor Back-Action Set Retractor Back-Action Set (5)
UDI device identifier 00083208133336 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208133336 |
|---|---|
| Brand name | DDP Retractor Back-Action Set |
| Version or model | Retractor Back-Action Set (5) |
| Catalog number | Retractor Back-Action Set (5) |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | EIG |
| GMDN term | Hand-held dental retractor |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 7, 2022 |
| Version date | Apr 15, 2022 |
| Description | Set of 4 Back-Action Retractors and 1 Back-Action Orban Knife and autoclavable cassette |
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: