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Pross Injectable Bone Void Filler - Taiwan Registration 1a22242bc8aaa78f535acabccf34a919

Access comprehensive regulatory information for Pross Injectable Bone Void Filler in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1a22242bc8aaa78f535acabccf34a919 and manufactured by SHINEO TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHINEO TECHNOLOGY CO., LTD..

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1a22242bc8aaa78f535acabccf34a919
Registration Details
Taiwan FDA Registration: 1a22242bc8aaa78f535acabccf34a919
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Device Details

Pross Injectable Bone Void Filler
TW: ไฟ่ซพๅฃซๅฏๆณจๅฐ„ๅž‹ไบบๅทฅ้ชจๅกซๅ……็‰ฉ
Risk Class 2
MD

Registration Details

1a22242bc8aaa78f535acabccf34a919

Ministry of Health Medical Device Manufacturing No. 005273

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

Mar 07, 2016

Mar 07, 2026