UDI device identifier
Alaris 2202-0007
UDI device identifier 10885403274039 · BD Switzerland Sàrl
Key facts
| Primary DI | 10885403274039 |
|---|---|
| Brand name | Alaris |
| Version or model | 2202-0007 |
| Catalog number | 2202-0007 |
| Company | BD Switzerland Sàrl |
| DUNS number | 482631558 |
| Product code | FPA |
| GMDN term | Electric infusion pump administration set, single-use |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 22, 2016 |
| Version date | Jun 29, 2023 |
| Description | Pump Infusion Set, 1.2 Micron Filter 309 cm (122 in) |
At a glance
- 10–99 MAUDE reports citing this UDI
- No 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: