UDI device identifier
GERSON 1730
UDI device identifier 00044585917308 · LOUIS M. GERSON CO.
Key facts
| Primary DI | 00044585917308 |
|---|---|
| Brand name | GERSON |
| Version or model | 1730 |
| Catalog number | 081730 |
| Company | LOUIS M. GERSON CO. |
| DUNS number | 001000363 |
| Product code | MSH |
| GMDN term | Surgical/medical respirator, non-antimicrobial, single-use |
| Premarket submission | K061375 |
| Device class | Class II |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jan 3, 2023 |
| Version date | Sep 20, 2024 |
| Description | 1730 Type N95 Particulate Respirator and Surgical Respirator |
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: