UDI device identifier
KIMGUARD™ KC200 Sterilization Wrap 68018
UDI device identifier 00036000680188 · KIMBERLY-CLARK GLOBAL SALES, LLC
Key facts
| Primary DI | 00036000680188 |
|---|---|
| Brand name | KIMGUARD™ KC200 Sterilization Wrap |
| Version or model | 68018 |
| Company | KIMBERLY-CLARK GLOBAL SALES, LLC |
| DUNS number | 830997032 |
| Product code | FRG |
| GMDN term | Sterilization packaging, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Nov 30, 2016 |
| Version date | Nov 8, 2019 |
| Description | 18"x 18"' Sterilization Wrap |
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: