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"Mindray" automatic external defibrillator and accessories - Taiwan Registration e99b83356201cb66e1f28f9ed96434b7

Access comprehensive regulatory information for "Mindray" automatic external defibrillator and accessories in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e99b83356201cb66e1f28f9ed96434b7 and manufactured by Shenzhen Mindray Bio-Medical Electronics Co., Ltd.. The authorized representative in Taiwan is Medone Medical Equipment Co., Ltd..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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e99b83356201cb66e1f28f9ed96434b7
Registration Details
Taiwan FDA Registration: e99b83356201cb66e1f28f9ed96434b7
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Device Details

"Mindray" automatic external defibrillator and accessories
TW: โ€œ้‚็‘žโ€่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จๅŠ้…ไปถ
Risk Class 3

Registration Details

e99b83356201cb66e1f28f9ed96434b7

DHA09200113103

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

E Cardiovascular Medicine Science

E.5310 ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ็ณป็ตฑ

Chinese goods;; input

Dates and Status

Apr 16, 2020

Apr 16, 2025