UDI device identifier
REPEATER H93813
UDI device identifier 00085412476513 · BAXTER CORPORATION ENGLEWOOD
Key facts
| Primary DI | 00085412476513 |
|---|---|
| Brand name | REPEATER |
| Version or model | H93813 |
| Catalog number | H93813 |
| Company | BAXTER CORPORATION ENGLEWOOD |
| DUNS number | 078383477 |
| Product code | FMF |
| GMDN term | Fluid transfer set, general-purpose |
| Premarket submission | K872743 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 23, 2016 |
| Version date | Feb 19, 2021 |
| Description | REPEATER Pump Fluid Transfer Tube Set, Non-Sterile |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 1,000+ 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: