UDI device identifier
Howard Leight Leight Sleepers
UDI device identifier 00033552016816 · SPERIAN HEARING PROTECTION, LLC
Key facts
| Primary DI | 00033552016816 |
|---|---|
| Brand name | Howard Leight |
| Version or model | Leight Sleepers |
| Catalog number | R-01681 |
| Company | SPERIAN HEARING PROTECTION, LLC |
| DUNS number | 014982953 |
| Product code | EWD |
| GMDN term | Earplugs, single-use |
| Device class | Unclassified |
| Single use | Yes |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Jul 31, 2020 |
| Version date | Jun 10, 2022 |
| Description | Leight Sleepers Single-Use Foam Earplugs, 20-Pairs |
At a glance
- None MAUDE reports citing this UDI
- No 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: