eudamed_udi
Primary ID: 05065006332185
EarPro (UDI 05065006332185)
Manufactured by LiquidPro Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EarPro - Primary ID 05065006332185
Device Regulatory Overview
The EarPro (Model/Catalog Number: Ear Pro® 0.5 ml) is a medical device manufactured by LiquidPro Ltd. This product is indexed under FDA Product Code / Category Classification Q030499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Ear Pro® 0.5 ml
- Product Code / EMDN
- Q030499
- Device Name
- EarPro® Waterproofing Ear Spray
- Database Sync Date
- 2026-08-09 16:49:21
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 EarPro?
The registered manufacturer of record for EarPro is LiquidPro Ltd.
What is the Primary UDI-DI identifier for EarPro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05065006332185.
What classification code is assigned to this device?
This device is registered under product classification code Q030499.
Similar Classification Devices (Q030499)
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