eudamed_udi
Primary ID: 06432100106254
Revaxör örondroppar med sköljblåsa (UDI 06432100106254)
Manufactured by Orion Oyj
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Revaxör örondroppar med sköljblåsa - Primary ID 06432100106254
Device Regulatory Overview
The Revaxör örondroppar med sköljblåsa (Model/Catalog Number: 163655) is a medical device manufactured by Orion Oyj. This product is indexed under FDA Product Code / Category Classification Q030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 163655
- Product Code / EMDN
- Q030499
- Device Name
- Remo-Wax
- Database Sync Date
- 2026-08-09 16:48:08
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 Revaxör örondroppar med sköljblåsa?
The registered manufacturer of record for Revaxör örondroppar med sköljblåsa is Orion Oyj.
What is the Primary UDI-DI identifier for Revaxör örondroppar med sköljblåsa?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06432100106254.
What classification code is assigned to this device?
This device is registered under product classification code Q030499.
Similar Classification Devices (Q030499)
Other Devices by Orion Oyj
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