UDI device identifier
KIMBERLY-CLARK® Fluidshield™ Fog-Free Procedure Mask with Visor 47147
UDI device identifier 00036000471472 · KIMBERLY-CLARK GLOBAL SALES, LLC
Key facts
| Primary DI | 00036000471472 |
|---|---|
| Brand name | KIMBERLY-CLARK® Fluidshield™ Fog-Free Procedure Mask with Visor |
| Version or model | 47147 |
| Company | KIMBERLY-CLARK GLOBAL SALES, LLC |
| DUNS number | 830997032 |
| Product code | FXX |
| GMDN term | Surgical/medical face mask, single-use |
| Premarket submission | K823078 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 30, 2016 |
| Version date | May 6, 2020 |
| Description | Procedure Mask with Visor |
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: