Relief Wax (UDI 301-030C)
Manufactured by Ortho Organizers, Inc.
Device Regulatory Overview
The Relief Wax (Model/Catalog Number: 301-030C) is a medical device manufactured by Ortho Organizers, Inc.. This product is indexed under FDA Product Code / Category Classification EGD within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 301-030C
- Product Code / EMDN
- EGD
- Device Name
- RELIEF WAX - RED CHERRY SCENT
- Database Sync Date
- 2026-08-09 09:01:40
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 Relief Wax?
The registered manufacturer of record for Relief Wax is Ortho Organizers, Inc..
What is the Primary UDI-DI identifier for Relief Wax?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 301-030C.
What classification code is assigned to this device?
This device is registered under product classification code EGD.
Similar Classification Devices (EGD)
Other Devices by Ortho Organizers, Inc.
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