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"Asia-Pacific Medical" fine mesh titanium bone plate system - Taiwan Registration b7b579bfd6eb72f2e62fef8b22305074

Access comprehensive regulatory information for "Asia-Pacific Medical" fine mesh titanium bone plate system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b7b579bfd6eb72f2e62fef8b22305074 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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b7b579bfd6eb72f2e62fef8b22305074
Registration Details
Taiwan FDA Registration: b7b579bfd6eb72f2e62fef8b22305074
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Device Details

"Asia-Pacific Medical" fine mesh titanium bone plate system
TW: โ€œไบžๅคช้†ซ็™‚โ€็ฒพๅพฎ็ถฒ็‹€้ˆฆ้ชจๆฟ็ณป็ตฑ
Risk Class 2

Registration Details

b7b579bfd6eb72f2e62fef8b22305074

DHY00500346502

Company Information

Taiwan, Province of China

Product Details

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

I General, Plastic Surgery and Dermatology

I.3300 Surgical mesh

Domestic

Dates and Status

Oct 05, 2011

Oct 05, 2026