UDI device identifier
Tincture of Benzoin Spray 4oz US 407000
UDI device identifier 00040565111827 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565111827 |
|---|---|
| Brand name | Tincture of Benzoin Spray 4oz US |
| Version or model | 407000 |
| Catalog number | 407000 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | FON |
| 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 | Tincture of Benzoin Skin Prep Spray is a skin prep spray that enhances the adhesion of tape/appliance while protecting sensitive skin from adhesives and body fluids. |
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: