Pure Global

"Philips" automatic external defibrillator - Taiwan Registration e87b7e7c58dcb979042f24febdf25efb

Access comprehensive regulatory information for "Philips" automatic external defibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e87b7e7c58dcb979042f24febdf25efb and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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.

Free Database
Powered by Pure Global AI
89,000+ Devices
e87b7e7c58dcb979042f24febdf25efb
Registration Details
Taiwan FDA Registration: e87b7e7c58dcb979042f24febdf25efb
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Philips" automatic external defibrillator
TW: โ€œ้ฃ›ๅˆฉๆตฆโ€ๅ•Ÿๅฟƒ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ
Risk Class 2
Cancelled

Registration Details

e87b7e7c58dcb979042f24febdf25efb

DHA00602283102

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.5310 ่‡ชๅ‹•้ซ”ๅค–ๅŽป้กซๅ™จ็ณป็ตฑ

import

Dates and Status

Oct 03, 2011

Oct 03, 2016

Apr 25, 2018

Cancellation Information

Logged out

่‡ช่กŒ้ตๅ…ฅ