UDI device identifier
AccuRelief ACRL-5200
UDI device identifier 00023601261007 · Drive Devilbiss Healthcare
Key facts
| Primary DI | 00023601261007 |
|---|---|
| Brand name | AccuRelief |
| Version or model | ACRL-5200 |
| Company | Drive Devilbiss Healthcare |
| DUNS number | 867673159 |
| Product code | PCC |
| GMDN term | Physical therapy transcutaneous neuromuscular electrical stimulation system |
| Premarket submission | K210364 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Dec 17, 2024 |
| Version date | May 27, 2026 |
| Description | AccuRelief Migraine TENS |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: