UDI device identifier
Dragonfly™ Duo
UDI device identifier 00183739000708 · LIGHTLAB IMAGING, INC.
Key facts
| Primary DI | 00183739000708 |
|---|---|
| Brand name | Dragonfly™ |
| Version or model | Duo |
| Catalog number | C408644 |
| Company | LIGHTLAB IMAGING, INC. |
| DUNS number | 018493531 |
| Product code | ORD |
| GMDN term | Coronary optical coherence tomography system catheter |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Apr 20, 2015 |
| Version date | Mar 29, 2018 |
| Description | Imaging Catheter |
At a glance
- 1–9 MAUDE reports citing this UDI
- No Linked premarket submission
- No EUDAMED counterpart found
- 1–9 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: