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"Philips" cardiac shock resuscitator - Taiwan Registration 8ddb2782fe384b3c9cffa32f0843dee6

Access comprehensive regulatory information for "Philips" cardiac shock resuscitator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 8ddb2782fe384b3c9cffa32f0843dee6 and manufactured by Philips Goldway (Shenzhen) Industrial Inc.. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including PHILIPS MEDICAL SYSTEMS, and 1 recent registrations in the same category. 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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8ddb2782fe384b3c9cffa32f0843dee6
Registration Details
Taiwan FDA Registration: 8ddb2782fe384b3c9cffa32f0843dee6
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Device Details

"Philips" cardiac shock resuscitator
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅฟƒ่‡Ÿ้›ปๆ“Šๅพฉ็”ฆๅ™จ
Risk Class 3

Registration Details

8ddb2782fe384b3c9cffa32f0843dee6

DHA09200106605

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

Input;; Chinese goods

Dates and Status

Sep 09, 2019

Sep 09, 2029

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