Cervix Brush.Cervical Cell Sampler (UDI 06973094411219)
Manufactured by Junocare Medical Devices Ltd
Device Regulatory Overview
The Cervix Brush.Cervical Cell Sampler (Model/Catalog Number: 92-0300-00) is a medical device manufactured by Junocare Medical Devices Ltd. This product is indexed under FDA Product Code / Category Classification U089002 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 92-0300-00
- Product Code / EMDN
- U089002
- Device Name
- Cervix Brush.Cervical Cell Sampler
- Database Sync Date
- 2026-08-09 16:46:23
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 Cervix Brush.Cervical Cell Sampler?
The registered manufacturer of record for Cervix Brush.Cervical Cell Sampler is Junocare Medical Devices Ltd.
What is the Primary UDI-DI identifier for Cervix Brush.Cervical Cell Sampler?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973094411219.
What classification code is assigned to this device?
This device is registered under product classification code U089002.
Similar Classification Devices (U089002)
Other Devices by Junocare Medical Devices Ltd
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