UDI device identifier
Enteral Feeding TL07019
UDI device identifier 00020451331560 · Medela LLC
Key facts
| Primary DI | 00020451331560 |
|---|---|
| Brand name | Enteral Feeding |
| Version or model | TL07019 |
| Company | Medela LLC |
| DUNS number | 052002029 |
| Product code | FPA |
| GMDN term | Intravenous administration tubing extension set |
| Premarket submission | K895367 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 20, 2017 |
| Version date | Sep 30, 2024 |
| Description | Bifurcated Enteral Extension Set, 70", Low Volume Minibore, Approx. Priming Vol. 1.90 mL, TwistLok |
At a glance
- None 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: