UDI device identifier
Gelfoam Plus 1503187
UDI device identifier 00085412095158 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412095158 |
|---|---|
| Brand name | Gelfoam Plus |
| Version or model | 1503187 |
| Catalog number | 1503187 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 628013963 |
| Product code | LMF |
| GMDN term | Collagen haemostatic agent, non-antimicrobial |
| Device class | Class III |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | Yes |
| Publish date | Sep 8, 2016 |
| Version date | Jul 21, 2023 |
| Description | GELFOAM® PLUS - COMPRESSED SPONGE is an implantable hemostat supplied as a ready to use medical device kit containing GELFOAM® Compressed Sterile Sponge, Thrombin Human lyophilized powder, two 10 mL Prefilled Saline Syringes 0.9 Percent Sodium Chloride Injection USP, and a Vial Access Device |
At a glance
- None MAUDE reports citing this UDI
- No 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: