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ReBorn Essence Venus Cervical Intervertebral Cage - Taiwan Registration 17bf38591a3faaa16ea1619ac92cec82

Access comprehensive regulatory information for ReBorn Essence Venus Cervical Intervertebral Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 17bf38591a3faaa16ea1619ac92cec82 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH CO., LTD..

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17bf38591a3faaa16ea1619ac92cec82
Registration Details
Taiwan FDA Registration: 17bf38591a3faaa16ea1619ac92cec82
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Device Details

ReBorn Essence Venus Cervical Intervertebral Cage
TW: โ€œ็‘žๅฏถๅ„„โ€็ถญ็ดๆ–ฏ้ ธๆคŽๆคŽ้–“่žๅˆๅ™จ
Risk Class 2
MD

Registration Details

17bf38591a3faaa16ea1619ac92cec82

Ministry of Health Medical Device Manufacturing No. 007719

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3080 Interbody fusion device

Produced in Taiwan, China

Dates and Status

Dec 20, 2022

Dec 20, 2027