UDI device identifier
FLOSEAL HEMOSTATIC MATRIX ADS201883
UDI device identifier 00085412656304 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412656304 |
|---|---|
| Brand name | FLOSEAL HEMOSTATIC MATRIX |
| Version or model | ADS201883 |
| Catalog number | ADS201883 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 628013963 |
| Product code | PMX |
| GMDN term | Collagen haemostatic agent, non-antimicrobial |
| Premarket submission | P990009 |
| Device class | Class III |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | May 31, 2019 |
| Version date | Aug 10, 2023 |
| Description | Floseal Matrix is indicated in surgical procedures (other than in ophthalmic) as an adjunct to hemostasis when control of bleeding by ligature or conventional procedures is ineffective or impractical. |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 10–99 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: