UDI device identifier
Aqua Lube Regular
UDI device identifier 00016169510045 · MAYER LABORATORIES, INC.
Key facts
| Primary DI | 00016169510045 |
|---|---|
| Brand name | Aqua Lube |
| Version or model | Regular |
| Catalog number | 51004 |
| Company | MAYER LABORATORIES, INC. |
| DUNS number | 175425982 |
| Product code | NUC |
| GMDN term | Sexual lubricant |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 15, 2016 |
| Version date | Aug 7, 2020 |
| Description | Personal Lubricant 4 fl. oz. |
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: