Pure Global
120408
III
Delisted

Defibrillator/Pacemakers, Externalๅค–้ƒจ้™ค้ขคๅ™จ/่ตทๆๅ™จ

This profile provides complete Hong Kong MDACS registration information for Defibrillator/Pacemakers, External. Review device classification, authorised representative (AR) details, manufacturer contacts, product codes, and regulatory milestones. Pure Global AI delivers bilingual transparency for medical device registrations across Asia.

Product Info: Defibrillator/Pacemakers, External

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Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
17882
State
N/A
Status
Delisted
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Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

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Manufacturer (่ฃฝ้€ ๅ•†)
Shenzhen Mindray Bio-Medical Electronics Co., Ltd.
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China
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Mindray Building, Keji 12th Road South, Hi-tech Industrial Park, Nanshan, 518057 Shenzhen, China
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Authorised Representative (AR)
Regulatory Timeline
Registration Date
November 14, 2012
Expiry Date
November 14, 2017
Delist Date
August 06, 2018
Remarks
Delisted.
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Product Models
BeneHeart D3