gudid
Primary ID: 1
SenzAway (UDI 1)
Manufactured by MAJESTIC DRUG CO. INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SenzAway - Primary ID 1
Device Regulatory Overview
The SenzAway (Model/Catalog Number: 1) is a medical device manufactured by MAJESTIC DRUG CO. INC.. This product is indexed under FDA Product Code / Category Classification LBH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1
- Product Code / EMDN
- LBH
- Device Name
- SenzAway is a gel designed to relieve sensitivity of teeth to cold, sweet and hot food and liquids. One application should relieve sensitivity of teeth immediately and will last at least three months (individual results may vary)
- Database Sync Date
- 2026-08-09 09:00:34
Full Regulatory Attributes
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{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of SenzAway?
The registered manufacturer of record for SenzAway is MAJESTIC DRUG CO. INC..
What is the Primary UDI-DI identifier for SenzAway?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1.
What classification code is assigned to this device?
This device is registered under product classification code LBH.
Similar Classification Devices (LBH)
Other Devices by MAJESTIC DRUG CO. INC.
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