120104
III
Expired.
Defibrillator/Pacemakers, External้ค้ขคๅจ/่ตทๆๅจ,ๅค้จ
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
็ขๅ่ณ่จ๏ผ ้ค้ขคๅจ/่ตทๆๅจ,ๅค้จ
Device Overview
Hong Kong MDACS registration summary and classification details.
Risk Class
III
Product Code
17882
Product Code Detail
17882 Defibrillator/Pacemakers, External
State
Expired.
Status
N/A
Manufacturer (่ฃฝ้ ๅ)
Physio-Control, Inc.
Physio-Control, Inc.
United States
็พๅฝ
11811 Willows Road N.E., Redmond WA 98052, USA
11811 Willows Road N.E., Redmond WA 98052, USA
Authorised Representative (AR)
BioVibes Medical Limited
ๅปๅ็งๆๆ้ๅ
ฌๅธ
29120912
Regulatory Timeline
Registration Date
April 27, 2012
Expiry Date
April 27, 2017
Product Models
LIFEPAK 20e Defibrillator/Monitor (3202487, 3202488)
LIFEPAK 20e ้ค้ขคๅจ/็ๆคไปช (3202487, 3202488)