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"Avatek" lumbar intervertebral fusion system - Taiwan Registration 2baed78d00fe7b65a0019fb5a0f6976f

Access comprehensive regulatory information for "Avatek" lumbar intervertebral fusion system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2baed78d00fe7b65a0019fb5a0f6976f and manufactured by ALPHATEC SPINE INC.. 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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2baed78d00fe7b65a0019fb5a0f6976f
Registration Details
Taiwan FDA Registration: 2baed78d00fe7b65a0019fb5a0f6976f
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Device Details

"Avatek" lumbar intervertebral fusion system
TW: โ€œ้˜ฟไผๆณฐๅ…‹โ€่…ฐๆคŽๆคŽ้–“่žๅˆ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

2baed78d00fe7b65a0019fb5a0f6976f

DHA00602358604

Company Information

United States

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

May 22, 2012

May 22, 2017

Dec 13, 2019

Cancellation Information

Logged out

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