UDI device identifier
Howard Leight by Honeywell AquaSeal
UDI device identifier 00033552016847 · SPERIAN HEARING PROTECTION, LLC
Key facts
| Primary DI | 00033552016847 |
|---|---|
| Brand name | Howard Leight by Honeywell |
| Version or model | AquaSeal |
| Catalog number | R-01684 |
| Company | SPERIAN HEARING PROTECTION, LLC |
| DUNS number | 014982953 |
| Product code | EWD |
| GMDN term | Earplugs, single-use |
| Device class | Unclassified |
| Single use | No |
| Packaged sterile | No |
| Implantable | No |
| Publish date | Sep 11, 2020 |
| Version date | Jun 10, 2022 |
| Description | AquaSeal Water-Blocking Reusable Earplugs with Carrying Case, 2-Pairs Howard Leight by Honeywell AquaSeal Water-Blocking Reusable Earplugs are specially designed to help prevent swimmer's ear. Using a triple flange design, these earplugs create a series of low-pressure air pocket seals inside your… |
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: