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“SYNTEC” Steinmann wire - Taiwan Registration 58843812418be5fcbe5be1762f992a4c

Access comprehensive regulatory information for “SYNTEC” Steinmann wire in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 58843812418be5fcbe5be1762f992a4c 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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58843812418be5fcbe5be1762f992a4c
Registration Details
Taiwan FDA Registration: 58843812418be5fcbe5be1762f992a4c
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Device Details

“SYNTEC” Steinmann wire
TW: “亞太醫療”史氏骨針
Risk Class 2
MD

Registration Details

58843812418be5fcbe5be1762f992a4c

Ministry of Health Medical Device Manufacturing No. 007517

Company Information

Taiwan, Province of China

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedics

N3040 Smooth or threaded metal bone fixation

Produced in Taiwan, China

Dates and Status

Jul 27, 2022

Jul 27, 2027