UDI device identifier
ACTICOAT FLEX3 4" X 8" 66800417
UDI device identifier 00040565124858 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565124858 |
|---|---|
| Brand name | ACTICOAT FLEX3 4" X 8" |
| Version or model | 66800417 |
| Catalog number | 66800417 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | FRO |
| GMDN term | Wound-nonadherent dressing, absorbent, antimicrobial |
| Premarket submission | K083113 |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jul 16, 2020 |
| Version date | Sep 7, 2023 |
| Description | Silver coated anti-microbial barrier dressing |
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: