UDI device identifier
EXTENSION SET 2N3363
UDI device identifier 00085412639406 · BAXTER HEALTHCARE CORPORATION
Key facts
| Primary DI | 00085412639406 |
|---|---|
| Brand name | EXTENSION SET |
| Version or model | 2N3363 |
| Catalog number | 2N3363 |
| Company | BAXTER HEALTHCARE CORPORATION |
| DUNS number | 005083209 |
| Product code | FPA |
| GMDN term | Electric infusion pump administration set, single-use |
| Premarket submission | K210430 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Dec 21, 2021 |
| Version date | Dec 29, 2021 |
| Description | Light Resistant Micro-Volume Extension Set |
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: