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"AETREX" Limb orthosis (Non-Sterile) - Taiwan Registration 1612b68e339320f539870dafc911921c

Access comprehensive regulatory information for "AETREX" Limb orthosis (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 1612b68e339320f539870dafc911921c and manufactured by AETREX WORLDWIDE INC.. The authorized representative in Taiwan is Mingyo Global Inc..

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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1612b68e339320f539870dafc911921c
Registration Details
Taiwan FDA Registration: 1612b68e339320f539870dafc911921c
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Device Details

"AETREX" Limb orthosis (Non-Sterile)
TW: "ๆ„›ๅด”ๅ…‹ๅธ" ่‚ข้ซ”่ฃๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

1612b68e339320f539870dafc911921c

Ministry of Health Medical Device Import No. 017266

DHA09401726600

Company Information

United States

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Dec 12, 2016

Dec 12, 2021

Cancellation Information

Logged out

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