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“CeramOptec” Twister Fiber - Taiwan Registration d48a7e0ab4ac19ad1e2e4e807c185bd1

Access comprehensive regulatory information for “CeramOptec” Twister Fiber in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d48a7e0ab4ac19ad1e2e4e807c185bd1 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..

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d48a7e0ab4ac19ad1e2e4e807c185bd1
Registration Details
Taiwan FDA Registration: d48a7e0ab4ac19ad1e2e4e807c185bd1
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Device Details

“CeramOptec” Twister Fiber
TW: “賽瑞歐特”催斯特光纖
Risk Class 2
MD

Registration Details

d48a7e0ab4ac19ad1e2e4e807c185bd1

Ministry of Health Medical Device Import No. 030555

DHA05603055503

Company Information

Germany

Product Details

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

I General and plastic surgical devices

I4810 Lasers for general surgery, plastic surgery and dermatology

Imported from abroad

Dates and Status

Nov 16, 2017

Nov 16, 2022