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"Sérenowwas" is the intermediary director of Sérigride - Taiwan Registration 8fcabc848d7a5e5f4e6fe2354be865f5

Access comprehensive regulatory information for "Sérenowwas" is the intermediary director of Sérigride in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8fcabc848d7a5e5f4e6fe2354be865f5 and manufactured by Cerenovus, Inc.;; CERENOVUS, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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8fcabc848d7a5e5f4e6fe2354be865f5
Registration Details
Taiwan FDA Registration: 8fcabc848d7a5e5f4e6fe2354be865f5
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Device Details

"Sérenowwas" is the intermediary director of Sérigride
TW: “賽瑞諾華斯” 賽瑞格萊德中介導管
Risk Class 2

Registration Details

8fcabc848d7a5e5f4e6fe2354be865f5

DHA05603724408

Company Information

Mexico;;United States

Product Details

Details are as detailed as approved Chinese instructions

K Neuroscience;; E Cardiovascular Medicine Science

E.1250 Percutaneous catheters;; K.5600 Neurovascular mechanical clot removal device for the treatment of acute ischemic stroke

import

Dates and Status

Jul 11, 2024

Jul 11, 2029