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“BoniPlus” Bone Graft - Taiwan Registration 7046b15a852b6346db64a9ae62b87e9a

Access comprehensive regulatory information for “BoniPlus” Bone Graft in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7046b15a852b6346db64a9ae62b87e9a and manufactured by Heyi Technology Co., Ltd. Precision Factory. The authorized representative in Taiwan is MONTJADE ENGINEERING 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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7046b15a852b6346db64a9ae62b87e9a
Registration Details
Taiwan FDA Registration: 7046b15a852b6346db64a9ae62b87e9a
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Device Details

“BoniPlus” Bone Graft
TW: “寶凝加”骨填補物
Risk Class 2
MD

Registration Details

7046b15a852b6346db64a9ae62b87e9a

Ministry of Health Medical Device Manufacturing No. 006022

Company Information

Taiwan, Province of China

Product Details

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

N Orthopedic devices

N3045 Resorbed calcium salt bone cavity filling device

Produced in Taiwan, China

Dates and Status

Feb 07, 2018

Feb 07, 2028