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"OPED Asia-Pacific" Limb orthosis(Non-Sterile) - Taiwan Registration a551206da9014718f6e9a86c41ee25d1

Access comprehensive regulatory information for "OPED Asia-Pacific" 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 a551206da9014718f6e9a86c41ee25d1 and manufactured by ARROW MEDICAL LTD. The authorized representative in Taiwan is OPED ASIA-PACIFIC COMPANY LIMITED.

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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a551206da9014718f6e9a86c41ee25d1
Registration Details
Taiwan FDA Registration: a551206da9014718f6e9a86c41ee25d1
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Device Details

"OPED Asia-Pacific" Limb orthosis(Non-Sterile)
TW: "歐霈德亞太" 肢體裝具(未滅菌)
Risk Class 1
MD
Cancelled

Registration Details

a551206da9014718f6e9a86c41ee25d1

Ministry of Health Medical Device Import No. 015892

DHA09401589202

Company Information

United Kingdom

Product Details

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Nov 24, 2015

Nov 24, 2020

Aug 05, 2022

Cancellation Information

Logged out

未展延而逾期者