UDI device identifier
Bone Molder - Straight Bone Molder - Straight
UDI device identifier 00083208130120 · Suncoast Dental, Inc
Key facts
| Primary DI | 00083208130120 |
|---|---|
| Brand name | Bone Molder - Straight |
| Version or model | Bone Molder - Straight |
| Catalog number | Bone Molder - Straight |
| Company | Suncoast Dental, Inc |
| DUNS number | 078352849 |
| Product code | DZN |
| GMDN term | Osteotomy compression/distraction instrument |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 3, 2021 |
| Version date | Feb 11, 2021 |
| Description | Bone molder - used to compress bone in between dental Implants at time of placement |
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: