UDI device identifier
EndoMask Eclipse® Size #3 – 291030
UDI device identifier 00182151000624 · MERLYN ASSOCIATES, INC.
Key facts
| Primary DI | 00182151000624 |
|---|---|
| Brand name | EndoMask Eclipse® |
| Version or model | Size #3 – 291030 |
| Catalog number | 291030 |
| Company | MERLYN ASSOCIATES, INC. |
| DUNS number | 606864184 |
| Product code | CAE |
| GMDN term | Oropharyngeal airway, single-use |
| Device class | Class I |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | May 30, 2017 |
| Version date | Mar 29, 2018 |
| Description | Size #3, Single-use Silicone Laryngeal Mask EndoMask Eclipse® offers the same high quality design and the same silicone materials as reusable EndoMask Elite® in a single-use disposable model. It comprises a soft smooth cuff and a soft to medium rigid tube body. The product is packaged in individual… |
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: