UDI device identifier
McDavid MD31350-50090-L
UDI device identifier 00029369185388 · Shock Doctor, Inc.
Key facts
| Primary DI | 00029369185388 |
|---|---|
| Brand name | McDavid |
| Version or model | MD31350-50090-L |
| Company | Shock Doctor, Inc. |
| DUNS number | 795860220 |
| Product code | KYS |
| GMDN term | Orthotic insole, prefabricated, non-antimicrobial |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 1, 2026 |
| Version date | Sep 9, 2026 |
| Description | Shock absorbing heel cup |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: