Identity
- Trade Name
- Howard Leight by Honeywell FDA UDI
- Generic Name
- Earplugs, single-use FDA UDI
- Device Name
- Super Leight Corded Pre-Shaped Single-Use Foam Earplugs - 50 Pair Tub FDA UDI
- Model / Reference
- Super Leight FDA UDI
- Description
- Super Leight Corded Pre-Shaped Single-Use Foam Earplugs - 50 Pair Tub FDA UDI
Identifiers
- Catalog Number
- R-33333 FDA UDI
- Primary DI / UDI-DI
- 00033552333333 FDA UDI
- FDA Product Code
- EWD FDA UDI
- GMDN Term
- Earplugs, single-use FDA UDI
Classification
- Device Class
- U FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
No
FDA UDI
Over-the-Counter
Yes
FDA UDI
Convenience Kit
No
FDA UDI
Combination Product
No
FDA UDI
HCT/P
No
FDA UDI
Premarket Exempt
Yes
FDA UDI
Lot / Batch Number
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Earplugs, single-use
Howard Leight by Honeywell by Sperian Hearing Protection, Llc — Class U — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class U | Pending data |
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Manufacturer
- Manufacturer
- Sperian Hearing Protection, Llc
Sources (1)
- FDA UDI 7a5f09e7-ac71-4574-8060-b69d67ab5988 34 fields · synced May 31, 2026