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"Biosen Webster" Mobicar atrial diaphragmatic puncture needle - Taiwan Registration fa8a5806c7eb5e565304514e68617a4a

Access comprehensive regulatory information for "Biosen Webster" Mobicar atrial diaphragmatic puncture needle in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fa8a5806c7eb5e565304514e68617a4a and manufactured by GREATBATCH MEDICAL INC. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

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fa8a5806c7eb5e565304514e68617a4a
Registration Details
Taiwan FDA Registration: fa8a5806c7eb5e565304514e68617a4a
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Device Details

"Biosen Webster" Mobicar atrial diaphragmatic puncture needle
TW: โ€œ็™พๆญๆฃฎๅ‰ไผฏๅธ็‰นโ€ๆ‘ฉๆฏ”ๅกๆ–ฏๅฟƒๆˆฟไธญ่†ˆ็ฉฟๅˆบ้‡
Risk Class 2
Cancelled

Registration Details

fa8a5806c7eb5e565304514e68617a4a

DHA00602489601

Company Information

United States

Product Details

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

E Cardiovascular Medicine Science

E.1390 Casing needle

import

Dates and Status

May 17, 2013

May 17, 2018

Nov 04, 2019

Cancellation Information

Logged out

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