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"Philips" automatic extracorporeal cardiac defibrous fibrillator - Taiwan Registration cb64fe9f91a05aee5b0f40cef87ed87c

Access comprehensive regulatory information for "Philips" automatic extracorporeal cardiac defibrous fibrillator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number cb64fe9f91a05aee5b0f40cef87ed87c and manufactured by PHILIPS MEDICAL SYSTEMS. The authorized representative in Taiwan is PHILIPS TAIWAN LIMITED.

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cb64fe9f91a05aee5b0f40cef87ed87c
Registration Details
Taiwan FDA Registration: cb64fe9f91a05aee5b0f40cef87ed87c
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Device Details

"Philips" automatic extracorporeal cardiac defibrous fibrillator
TW: "้ฃ›ๅˆฉๆตฆ"่‡ชๅ‹•้ซ”ๅค–ๅฟƒ่‡ŸๅŽป็บ–็ถญ้กซๅ‹•ๅ™จ
Risk Class 3
Cancelled

Registration Details

cb64fe9f91a05aee5b0f40cef87ed87c

DHA00600904807

Company Information

United States

Product Details

0699 Other Intensive Care Unit & Cardiac Care Unit Equipment

import

Dates and Status

Nov 13, 2012

Feb 09, 2019

Jul 15, 2022

Cancellation Information

Logged out

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