UDI device identifier
SPECTRUM WITH MDL 35700BAX
UDI device identifier 00085412091570 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412091570 |
|---|---|
| Brand name | SPECTRUM WITH MDL |
| Version or model | 35700BAX |
| Catalog number | 35700BAX |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 079209157 |
| Product code | FRN |
| GMDN term | Bedside infusion pump, single-channel |
| Device class | Class II |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Oct 19, 2022 |
| Description | The Spectrum infusion pump consists of electronic circuitry and mechanisms in a plastic enclosure. The operation is software controlled, with linear peristaltic pumping design. The Spectrum is designed for the application of standard gravity infusion sets as indicated by the Spectrums labeling. |
At a glance
- 100–999 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: