UDI device identifier
Exeltra Dialyzer 150
UDI device identifier 00085412071275 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412071275 |
|---|---|
| Brand name | Exeltra Dialyzer |
| Version or model | 150 |
| Catalog number | 5M2119 |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 005146311 |
| Product code | KDI |
| GMDN term | Hollow-fibre haemodialysis dialyser, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Oct 12, 2015 |
| Version date | Aug 30, 2023 |
| Description | Hemodialysis with EXELTRA and EXELTRA Plus dialyzers is indicated for patients with acute or chronic renal failure when conservative therapy is judged to be inadequate. It also may be indicated in the treatment of patients intoxicated with poisons or drugs. |
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: