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“SYNTEC” Halo System (Non-Sterile) - Taiwan Registration 94c4bfe3ebbd73c3c77b9bc08ffbda98

Access comprehensive regulatory information for “SYNTEC” Halo System (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 94c4bfe3ebbd73c3c77b9bc08ffbda98 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.

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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94c4bfe3ebbd73c3c77b9bc08ffbda98
Registration Details
Taiwan FDA Registration: 94c4bfe3ebbd73c3c77b9bc08ffbda98
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Device Details

“SYNTEC” Halo System (Non-Sterile)
TW: “亞太”胸頸護架 (未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

94c4bfe3ebbd73c3c77b9bc08ffbda98

Ministry of Health Medical Device Manufacturing Registration No. 001970

DHY08300197009

Company Information

Taiwan, Province of China

Product Details

o Equipment for physical medicine

O3490 Torso Gear

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

未展延而逾期者