UDI device identifier
Shiley 7CN80R
UDI device identifier 10884521205444 · Covidien LP
Key facts
| Primary DI | 10884521205444 |
|---|---|
| Brand name | Shiley |
| Version or model | 7CN80R |
| Company | Covidien LP |
| DUNS number | 058614483 |
| Product code | JOH |
| GMDN term | Tracheostomy tube, non-reinforced, non-customized, single-use |
| Premarket submission | K150844 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Jul 16, 2026 |
| Description | Adult Flexible Tracheostomy Tube with TaperGuard (TM) Cuff Reusable Inner Cannula |
At a glance
- 1–9 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: