Automated External Defibrillator (UDI 06936415912413)
Manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
Device Regulatory Overview
The Automated External Defibrillator (Model/Catalog Number: /) is a medical device manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12030501 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- Z12030501
- Device Name
- Automated External Defibrillator
- Database Sync Date
- 2026-08-09 16:47:01
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 Automated External Defibrillator?
The registered manufacturer of record for Automated External Defibrillator is Shenzhen Mindray Bio-Medical Electronics Co., Ltd..
What is the Primary UDI-DI identifier for Automated External Defibrillator?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06936415912413.
What classification code is assigned to this device?
This device is registered under product classification code Z12030501.
Similar Classification Devices (Z12030501)
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