UDI device identifier
INTERLINK 2C1103
UDI device identifier 00085412000503 · BAXTER INTERNATIONAL INC.
Key facts
| Primary DI | 00085412000503 |
|---|---|
| Brand name | INTERLINK |
| Version or model | 2C1103 |
| Catalog number | 2C1103 |
| Company | BAXTER INTERNATIONAL INC. |
| DUNS number | 005146311 |
| Product code | FPA |
| GMDN term | Intravenous line filter |
| Premarket submission | K952074 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 24, 2016 |
| Version date | Jul 6, 2018 |
| Description | Non-DEHP Extension Set with 1.2 Micron Downstream Filter, Air Eliminating Filter, INTERLINK Injection Site |
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: