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Sindis Power Surgery Kit - Taiwan Registration 2ddded500e15fdbd2d030ef0a33009ab

Access comprehensive regulatory information for Sindis Power Surgery Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2ddded500e15fdbd2d030ef0a33009ab and manufactured by SYNTHES. The authorized representative in Taiwan is Taiwan Sindis Medical Equipment Co., Ltd.

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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2ddded500e15fdbd2d030ef0a33009ab
Registration Details
Taiwan FDA Registration: 2ddded500e15fdbd2d030ef0a33009ab
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Device Details

Sindis Power Surgery Kit
TW: ไฟก่ฟชๆ€ๅ‹•ๅŠ›ๆ‰‹่ก“ๅทฅๅ…ท็ต„
Risk Class 1
Cancelled

Registration Details

2ddded500e15fdbd2d030ef0a33009ab

DHA04400295907

Company Information

Switzerland

Product Details

This device is a surgical instrument, the motor and accessories are equipment that uses alternating current, dry batteries, or air power, and is intended to provide electricity during surgery to operate various accessories or accessories to cut hard tissues, bones, and soft tissues. Accessories or accessories include: tweezers, chisels (bone cutters), skin scrubs, skin cutters, small drills, hammer heads, needle starters, scapular saws.

I General, Plastic Surgery and Dermatology

import

Dates and Status

Mar 15, 2006

Mar 15, 2011

Jan 21, 2013

Cancellation Information

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