Dopplo (UDI 06973912940051)
Manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.
Device Regulatory Overview
The Dopplo (Model/Catalog Number: YM2T925502) is a medical device manufactured by Shenzhen IMDK Medical Technology Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification Z12080103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- YM2T925502
- Product Code / EMDN
- Z12080103
- Device Name
- Ultrasonic Doppler Fetal Heart Rate Detector
- Database Sync Date
- 2026-08-09 18:44:16
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 Dopplo?
The registered manufacturer of record for Dopplo is Shenzhen IMDK Medical Technology Co.,Ltd..
What is the Primary UDI-DI identifier for Dopplo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06973912940051.
What classification code is assigned to this device?
This device is registered under product classification code Z12080103.
Similar Classification Devices (Z12080103)
Other Devices by Shenzhen IMDK Medical Technology Co.,Ltd.
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