UDI device identifier
LVAD 1/4 BEQ-T 3502
UDI device identifier 00060756720676 · DATASCOPE CORP.
Key facts
| Primary DI | 00060756720676 |
|---|---|
| Brand name | LVAD 1/4 |
| Version or model | BEQ-T 3502 |
| Catalog number | 701068168 |
| Company | DATASCOPE CORP. |
| DUNS number | 001660786 |
| Product code | DWE |
| GMDN term | Cardiopulmonary bypass system blood tubing set |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 28, 2016 |
| Version date | Dec 8, 2022 |
| Description | Softshell Venous Reser. 800ml, BEQ-RF32 RotaFlow, HPH 400, CDI Sat Cell 1/4" System 100, Blood Microfilter System SQ 40 S, |
At a glance
- None MAUDE reports citing this UDI
- No 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: