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"Artis" vascular examiner - Taiwan Registration 6ff0dff14cc5d1de3050d2e7e868d19f

Access comprehensive regulatory information for "Artis" vascular examiner in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ff0dff14cc5d1de3050d2e7e868d19f and manufactured by ATYS MEDICAL. The authorized representative in Taiwan is NIEN TAI MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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6ff0dff14cc5d1de3050d2e7e868d19f
Registration Details
Taiwan FDA Registration: 6ff0dff14cc5d1de3050d2e7e868d19f
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Device Details

"Artis" vascular examiner
TW: "ไบžๆๆ–ฏ"่ก€็ฎกๆชขๆŸฅๅ„€
Risk Class 2
Cancelled

Registration Details

6ff0dff14cc5d1de3050d2e7e868d19f

DHA00601697600

Company Information

France

Product Details

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

E Cardiovascular Medicine Science

E.2780 ๆถฒๅฃ“.ใ€ๆฐฃๅฃ“ๆˆ–ๅ…‰้›ปๅผ้ซ”็ฉๆ่จ˜ๅ™จ

import

Dates and Status

Aug 08, 2006

Aug 08, 2021

Aug 28, 2023

Cancellation Information

Logged out

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