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GEZEN Lumbar Cage - Taiwan Registration 4f6fca5f453c8ad4275f51d16050a3a4

Access comprehensive regulatory information for GEZEN Lumbar Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4f6fca5f453c8ad4275f51d16050a3a4 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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4f6fca5f453c8ad4275f51d16050a3a4
Registration Details
Taiwan FDA Registration: 4f6fca5f453c8ad4275f51d16050a3a4
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Device Details

GEZEN Lumbar Cage
TW: ้š›ไป่…ฐๆคŽ่žๅˆ่ฃ็ฝฎ
Risk Class 2
MD

Registration Details

4f6fca5f453c8ad4275f51d16050a3a4

Ministry of Health Medical Device Manufacturing No. 005445

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

Aug 24, 2016

Aug 24, 2026