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“SYNTEC” D Fit-Titanium Vertebral Interbody Cage - Taiwan Registration 48addd0c6e08c1e56ac2be579cfa3780

Access comprehensive regulatory information for “SYNTEC” D Fit-Titanium Vertebral Interbody Cage in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 48addd0c6e08c1e56ac2be579cfa3780 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.

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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48addd0c6e08c1e56ac2be579cfa3780
Registration Details
Taiwan FDA Registration: 48addd0c6e08c1e56ac2be579cfa3780
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Device Details

“SYNTEC” D Fit-Titanium Vertebral Interbody Cage
TW: “亞太醫療”雙合-鈦合金椎間融合器
Risk Class 2
MD

Registration Details

48addd0c6e08c1e56ac2be579cfa3780

Ministry of Health Medical Device Manufacturing No. 006693

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

May 06, 2020

May 06, 2025