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"Philips" cardiac shock resuscitator - Taiwan Registration 473d5b8f8ee9b0196a58ca671bbb9c51

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 2 medical device is registered under number 473d5b8f8ee9b0196a58ca671bbb9c51 and manufactured by PHILIPS MEDICAL SYSTEMS. 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 Goldway (Shenzhen) Industrial Inc., 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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473d5b8f8ee9b0196a58ca671bbb9c51
Registration Details
Taiwan FDA Registration: 473d5b8f8ee9b0196a58ca671bbb9c51
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Device Details

"Philips" cardiac shock resuscitator
TW: "้ฃ›ๅˆฉๆตฆ"ๅฟƒ่‡Ÿ้›ปๆ“Šๅพฉ็”ฆๅ™จ
Risk Class 2
Cancelled

Registration Details

473d5b8f8ee9b0196a58ca671bbb9c51

DHA00600823004

Company Information

United States

Product Details

๏ผŽ

0600 Intensive Care Unit and Cardiac Intensive Care Unit Equipment

import

Dates and Status

Apr 16, 1997

Feb 09, 2019

Jul 15, 2022

Cancellation Information

Logged out

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