UDI device identifier
ULTRA 4"x5"
UDI device identifier 00015961293026 · MILLIKEN HEALTHCARE PDTS, LLC
Key facts
| Primary DI | 00015961293026 |
|---|---|
| Brand name | ULTRA |
| Version or model | 4"x5" |
| Catalog number | 3000006840 |
| Company | MILLIKEN HEALTHCARE PDTS, LLC |
| DUNS number | 963905539 |
| Product code | NAD |
| GMDN term | Exudate-absorbent dressing, non-gel, non-antimicrobial |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Jan 6, 2021 |
| Version date | Jun 22, 2021 |
| Description | ULTRA is a sterile, single use foam wound dressing. ULTRA is indicated for low to highly exuding acute and chronic wounds such as partial thickness burns, incisions, skin grafts, donor sites, lacerations, abrasions, and stage I-IV pressure ulcers, venous ulcers, and diabetic ulcers. The dressing has… |
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: