UDI device identifier
Poise Pessary
UDI device identifier 00036000465600 · KIMBERLY-CLARK GLOBAL SALES, INC.
Key facts
| Primary DI | 00036000465600 |
|---|---|
| Brand name | Poise |
| Version or model | Pessary |
| Company | KIMBERLY-CLARK GLOBAL SALES, INC. |
| DUNS number | 829568273 |
| Product code | HHW |
| GMDN term | Urinary-incontinence vaginal insert, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Apr 5, 2019 |
| Version date | Jan 8, 2025 |
| Description | POISE IMPRESSA SIZE 3 BLADDER SUPPORT DEVICE |
At a glance
- 1–9 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: