UDI device identifier
ALIF Disc Prep 106.7070
UDI device identifier 00008417321664 · CTL Medical Corporation
Key facts
| Primary DI | 00008417321664 |
|---|---|
| Brand name | ALIF Disc Prep |
| Version or model | 106.7070 |
| Company | CTL Medical Corporation |
| DUNS number | 080138504 |
| Product code | MAX |
| GMDN term | General internal orthopaedic fixation system implantation kit |
| Premarket submission | K192863 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 30, 2024 |
| Version date | Nov 21, 2024 |
| Description | Wedge Distractor Inserter |
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: