Doppler FHR Detector (UDI 06937492645065)
Manufactured by Shenzhen Bestman Instrument Co., Ltd.
Device Regulatory Overview
The Doppler FHR Detector (Model/Catalog Number: /) is a medical device manufactured by Shenzhen Bestman Instrument 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
- /
- Product Code / EMDN
- Z12080103
- Device Name
- Ultrasound Series Doppler FHR Detectors
- Database Sync Date
- 2026-08-09 17:08:07
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 Doppler FHR Detector?
The registered manufacturer of record for Doppler FHR Detector is Shenzhen Bestman Instrument Co., Ltd..
What is the Primary UDI-DI identifier for Doppler FHR Detector?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06937492645065.
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 Bestman Instrument Co., Ltd.
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