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Bone wire - Taiwan Registration 82f6df23b99b51c0f50b3495746e97f6

Access comprehensive regulatory information for Bone wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 82f6df23b99b51c0f50b3495746e97f6 and manufactured by SYNTEC SCIENTIFIC CORPORATION. The authorized representative in Taiwan is SYNTEC SCIENTIFIC CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 3 companies making similar products including SMITH & NEPHEW RICHAROS INC., RICHARDS MANUFACTURING GMBH, and 4 recent registrations in the same category. 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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82f6df23b99b51c0f50b3495746e97f6
Registration Details
Taiwan FDA Registration: 82f6df23b99b51c0f50b3495746e97f6
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Device Details

Bone wire
TW: ้ชจ้‹ผ็ตฒ
Risk Class 2

Registration Details

82f6df23b99b51c0f50b3495746e97f6

DHY00500073006

Company Information

Taiwan, Province of China

Product Details

0305 Artificial bone needles

Domestic

Dates and Status

Aug 28, 1998

Aug 28, 2028