UDI device identifier
Enteral Feeding NTL10
UDI device identifier 00020451330969 · Medela LLC
Key facts
| Primary DI | 00020451330969 |
|---|---|
| Brand name | Enteral Feeding |
| Version or model | NTL10 |
| Company | Medela LLC |
| DUNS number | 052002029 |
| Product code | FMF |
| GMDN term | ENFit oral/enteral syringe, single-use |
| Premarket submission | K092986 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 20, 2017 |
| Version date | Sep 30, 2024 |
| Description | Enteral Syringe 10mL, 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: