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GEZEN Cervical Cage - Taiwan Registration c64c46158178864db5b0f7fc4fd19f7b

Access comprehensive regulatory information for GEZEN Cervical Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number c64c46158178864db5b0f7fc4fd19f7b and manufactured by BIOLIFE MEDICAL DEVICE INC.. The authorized representative in Taiwan is BIOLIFE MEDICAL DEVICE 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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c64c46158178864db5b0f7fc4fd19f7b
Registration Details
Taiwan FDA Registration: c64c46158178864db5b0f7fc4fd19f7b
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Device Details

GEZEN Cervical Cage
TW: ้š›ไป้ ธๆคŽ่žๅˆ่ฃ็ฝฎ
Risk Class 2
MD

Registration Details

c64c46158178864db5b0f7fc4fd19f7b

Ministry of Health Medical Device Manufacturing No. 005384

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3080 Interbody fusion device

Produced in Taiwan, China

Dates and Status

Jul 19, 2016

Jul 19, 2026