UDI device identifier
TheraTouch SW1 CR15-APP
UDI device identifier 00092237626955 · Drive Devilbiss Healthcare
Key facts
| Primary DI | 00092237626955 |
|---|---|
| Brand name | TheraTouch SW1 |
| Version or model | CR15-APP |
| Company | Drive Devilbiss Healthcare |
| DUNS number | 867673159 |
| Product code | ISA |
| GMDN term | Multidisciplinary extracorporeal shock wave therapy system, mobile |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 4, 2025 |
| Version date | May 27, 2026 |
| Description | Shockwave CR 15mm Applicator |
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: