UDI device identifier
3M™ Nexcare™ SLT-SIOC
UDI device identifier 00051131216136 · 3M COMPANY
Key facts
| Primary DI | 00051131216136 |
|---|---|
| Brand name | 3M™ Nexcare™ |
| Version or model | SLT-SIOC |
| Catalog number | SLT-SIOC |
| Company | 3M COMPANY |
| DUNS number | 830016148 |
| Product code | KGX |
| GMDN term | Hypoallergenic skin adhesive tape |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 25, 2018 |
| Version date | Oct 23, 2019 |
| Description | Nexcare™ Sensitive Skin Tape SLT-SIOC, 1 in x 4 yd (25,4 mm x 3,65 m), 6 pack |
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: