UDI device identifier
Aleve 1613538
UDI device identifier 00016500574057 · BAYER HEALTHCARE LLC
Key facts
| Primary DI | 00016500574057 |
|---|---|
| Brand name | Aleve |
| Version or model | 1613538 |
| Company | BAYER HEALTHCARE LLC |
| DUNS number | 112117283 |
| Product code | NUH |
| GMDN term | Analgesic transcutaneous electrical nerve stimulation system |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 1, 2017 |
| Version date | Oct 23, 2019 |
| Description | Aleve Direct Therapy TENS Device delivers stimulating pulses to the site of pain using the same technology found in doctors, physical therapists, and chiropractor's offices. Aleve Direct Therapy TENS Device is indicated for temporary relief of pain associated with sore and aching muscles in the… |
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: