UDI device identifier
Premixed Dialysate for Hemodiafiltration 5B7860
UDI device identifier 00085412007380 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412007380 |
|---|---|
| Brand name | Premixed Dialysate for Hemodiafiltration |
| Version or model | 5B7860 |
| Catalog number | 5B7860 |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 005146311 |
| Product code | KPO |
| GMDN term | Haemodialysis concentrate |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 24, 2015 |
| Version date | Jul 21, 2023 |
| Description | Premixed Dialysate for Hemodiafiltration is indicated for acute dialysis modalities that employ hemodiafiltration, such as continuous arteriovenous hemodiafiltration (CAVHD) and Continuous Venous-Venous Hemodiafiltration (CVVHD), when treatment of acute renal failure patients with hypervolemia and… |
At a glance
- None MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: