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ReBorn Essence LIF-PISCES Vertebral Spacer - Taiwan Registration 967be331f3ebbff26461cbf73578ba38

Access comprehensive regulatory information for ReBorn Essence LIF-PISCES Vertebral Spacer in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 967be331f3ebbff26461cbf73578ba38 and manufactured by BAUI BIOTECH CO., LTD.. The authorized representative in Taiwan is BAUI BIOTECH 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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967be331f3ebbff26461cbf73578ba38
Registration Details
Taiwan FDA Registration: 967be331f3ebbff26461cbf73578ba38
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Device Details

ReBorn Essence LIF-PISCES Vertebral Spacer
TW: โ€œ็‘žๅฏถๅ„„โ€ๅธ•่ฅฟๆ–ฏๆคŽ้ซ”ๆ”ฏๆŸฑๅกŠ
Risk Class 2
MD

Registration Details

967be331f3ebbff26461cbf73578ba38

Ministry of Health Medical Device Manufacturing No. 006309

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

Dec 17, 2018

Dec 17, 2028