UDI device identifier
therMaxTherMax Blood Warmer 955630
UDI device identifier 00085412639505 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412639505 |
|---|---|
| Brand name | therMaxTherMax Blood Warmer |
| Version or model | 955630 |
| Catalog number | 955630 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 005083209 |
| Product code | KDI |
| GMDN term | Conduction blood/fluid warmer |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 31, 2020 |
| Version date | Apr 21, 2025 |
| Description | The TherMax blood warmer is an accessory device intended for use with the PrisMax system and appropriate blood warmer compatible Prismaflex sets for the therapy in use. The blood warmer heats the return blood flow during a PrisMax system treatment in order to replace heat lost to the atmosphere and… |
At a glance
- 1–9 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: