UDI device identifier
Astroglide Quiver 015594011967
UDI device identifier 00015594011967 · BIOFILM, INC
Key facts
| Primary DI | 00015594011967 |
|---|---|
| Brand name | Astroglide Quiver |
| Version or model | 015594011967 |
| Company | BIOFILM, INC |
| DUNS number | 790780258 |
| Product code | HIS |
| GMDN term | Sexual lubricant |
| Premarket submission | K041432 |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Feb 15, 2022 |
| Version date | Jun 7, 2023 |
| Description | Astroglide Quiver is a personal lubricant for penile, vaginal and/or anal application intended to moisturize and lubricate, to enhance the ease and comfort of sexual activity and supplement the body's natural lubrication. This product is compatible with natural rubber latex and polyisoprene condoms… |
At a glance
- None MAUDE reports citing this UDI
- Yes 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: