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"Dai Max" Seri Ultrasound Imaging System - Taiwan Registration 7bb433b26f1d9361424830b14b5b5d65

Access comprehensive regulatory information for "Dai Max" Seri Ultrasound Imaging System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7bb433b26f1d9361424830b14b5b5d65 and manufactured by DYMAX CORPORATION. The authorized representative in Taiwan is BARD PACIFIC HEALTH CARE CO., LTD..

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7bb433b26f1d9361424830b14b5b5d65
Registration Details
Taiwan FDA Registration: 7bb433b26f1d9361424830b14b5b5d65
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Device Details

"Dai Max" Seri Ultrasound Imaging System
TW: "ๆˆด้บฅๅ…‹ๆ€" ็‘Ÿ็‘ž่ถ…้Ÿณๆณขๅฝฑๅƒ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

7bb433b26f1d9361424830b14b5b5d65

DHA00601367204

Company Information

United States

Product Details

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

P Radiology Science

import

Dates and Status

Nov 24, 2005

Nov 24, 2015

May 28, 2018

Cancellation Information

Logged out

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