UDI device identifier
Repair-It 1
UDI device identifier 00010705400913 · MAJESTIC DRUG CO. INC.
Key facts
| Primary DI | 00010705400913 |
|---|---|
| Brand name | Repair-It |
| Version or model | 1 |
| Company | MAJESTIC DRUG CO. INC. |
| DUNS number | 001496777 |
| Product code | EBO |
| GMDN term | Denture repair kit, home-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 27, 2016 |
| Version date | Nov 6, 2020 |
| Description | Repair-It Advanced Denture Repair Kit repairs broken dentures and denture teeth in minutes: Fix breaks, replace loose teeth, and mend cracks. |
At a glance
- 1–9 MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: