UDI device identifier
REPLICaRE ULTRa SaCRUM 59484900
UDI device identifier 00040565120799 · SMITH & NEPHEW MEDICAL LIMITED
Key facts
| Primary DI | 00040565120799 |
|---|---|
| Brand name | REPLICaRE ULTRa SaCRUM |
| Version or model | 59484900 |
| Catalog number | 59484900 |
| Company | SMITH & NEPHEW MEDICAL LIMITED |
| DUNS number | 216344051 |
| Product code | NAD |
| GMDN term | Exudate-absorbent dressing, hydrophilic-gel, non-antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 7, 2020 |
| Version date | Sep 7, 2023 |
| Description | Advanced hydrocolloid dressing |
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: