UDI device identifier
Adult Specialty Pack BEQ-TOP 40800
UDI device identifier 00060756720454 · DATASCOPE CORP.
Key facts
| Primary DI | 00060756720454 |
|---|---|
| Brand name | Adult Specialty Pack |
| Version or model | BEQ-TOP 40800 |
| Catalog number | 701062913 |
| 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 | BEQ-HMOD 70000-USA Adult Quadrox iD, FlowProbe Connector, Gas Filter |
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: