UDI device identifier
H93835
UDI device identifier 00085412476551 · BAXTER CORPORATION ENGLEWOOD
Key facts
| Primary DI | 00085412476551 |
|---|---|
| Version or model | H93835 |
| Catalog number | H93835 |
| Company | BAXTER CORPORATION ENGLEWOOD |
| DUNS number | 078383477 |
| Product code | LHI |
| GMDN term | Laboratory syringe filter |
| Premarket submission | K900585 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | Yes |
| Implantable | No |
| Publish date | Sep 23, 2016 |
| Version date | Jul 6, 2018 |
| Description | Sterile 0.2 Micron Filter |
At a glance
- None MAUDE reports citing this UDI
- Yes Linked premarket submission
- No EUDAMED counterpart found
- 100–999 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: