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"Guanya" hynix lumbar intervertebral fusion device - Taiwan Registration d4a5c1962f510bcc4ffef7b9b3312791

Access comprehensive regulatory information for "Guanya" hynix lumbar intervertebral 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 d4a5c1962f510bcc4ffef7b9b3312791 and manufactured by A-SPINE Asia Co., Ltd.. The authorized representative in Taiwan is A-SPINE Asia 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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d4a5c1962f510bcc4ffef7b9b3312791
Registration Details
Taiwan FDA Registration: d4a5c1962f510bcc4ffef7b9b3312791
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Device Details

"Guanya" hynix lumbar intervertebral fusion device
TW: "ๅ† ไบž" ๆตทๅŠ›ๅฃซ่…ฐๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
Cancelled

Registration Details

d4a5c1962f510bcc4ffef7b9b3312791

DHY00500133709

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedics

Domestic

Dates and Status

May 03, 2005

May 03, 2020

Jun 07, 2022

Cancellation Information

Logged out

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