UDI device identifier
REMOVE Adhesive Remover 8oz US 403300
UDI device identifier 00040565112435 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565112435 |
|---|---|
| Brand name | REMOVE Adhesive Remover 8oz US |
| Version or model | 403300 |
| Catalog number | 403300 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | KOX |
| GMDN term | Patient medical adhesive remover |
| Device class | Class I |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 4, 2020 |
| Version date | Sep 7, 2023 |
| Description | Universal adhesive remover spray |
At a glance
- 1–9 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: