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"Sains" lumbar fusion device - Taiwan Registration 937af7ba03211734bde70efde3e461ab

Access comprehensive regulatory information for "Sains" lumbar fusion device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 937af7ba03211734bde70efde3e461ab and manufactured by Scient'x S.A.S. The authorized representative in Taiwan is K&C MEDICAL 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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937af7ba03211734bde70efde3e461ab
Registration Details
Taiwan FDA Registration: 937af7ba03211734bde70efde3e461ab
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Device Details

"Sains" lumbar fusion device
TW: โ€œ่ณฝๆฉๅธโ€่…ฐๆคŽ่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

937af7ba03211734bde70efde3e461ab

DHA00602113806

Company Information

France

Product Details

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

N Orthopedics

N.3060 ๆคŽ้ซ”้–“ไน‹่„ŠๆคŽ็Ÿฏๆญฃๅ›บๅฎš็‰ฉ

import

Dates and Status

Jun 18, 2010

Jun 18, 2020

Jun 22, 2022

Cancellation Information

Logged out

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