UDI device identifier
Poise Pad
UDI device identifier 00036000534498 · KIMBERLY-CLARK GLOBAL SALES, INC.
Key facts
| Primary DI | 00036000534498 |
|---|---|
| Brand name | Poise |
| Version or model | Pad |
| Company | KIMBERLY-CLARK GLOBAL SALES, INC. |
| DUNS number | 829568273 |
| Product code | HHD |
| GMDN term | Menstrual pad, unscented |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 1, 2020 |
| Version date | Sep 30, 2022 |
| Description | ONE BY POISE SUPRPREM ULTRATHN REGWNG PAD 22 |
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: