WUSH (UDI WUSH0106,WUSH0706,WUSH0906,WUSH0103,WUSH1012)
Manufactured by GUANGDONG OKAY TECHNOLOGY CO.,LTD.
Device Regulatory Overview
The WUSH (Model/Catalog Number: WUSH0106,WUSH0706,WUSH0906,WUSH0103,WUSH1012) is a medical device manufactured by GUANGDONG OKAY TECHNOLOGY CO.,LTD.. This product is indexed under FDA Product Code / Category Classification LRD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- WUSH0106,WUSH0706,WUSH0906,WUSH0103,WUSH1012
- Product Code / EMDN
- LRD
- Device Name
- Wush Powered Ear Cleaner,Black wolf-Wush Rechargeable (Basic, 6 tip, catch cup)This device complies with part 18 of FCC rules.
- Database Sync Date
- 2026-08-09 09:24:45
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 WUSH?
The registered manufacturer of record for WUSH is GUANGDONG OKAY TECHNOLOGY CO.,LTD..
What is the Primary UDI-DI identifier for WUSH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WUSH0106,WUSH0706,WUSH0906,WUSH0103,WUSH1012.
What classification code is assigned to this device?
This device is registered under product classification code LRD.
Similar Classification Devices (LRD)
Other Devices by GUANGDONG OKAY TECHNOLOGY CO.,LTD.
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