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Leonardo Dual Laser System - Taiwan Registration fc0db080ed505bf4c9f04ddf98229b75

Access comprehensive regulatory information for Leonardo Dual Laser System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fc0db080ed505bf4c9f04ddf98229b75 and manufactured by CeramOptec GmbH. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..

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fc0db080ed505bf4c9f04ddf98229b75
Registration Details
Taiwan FDA Registration: fc0db080ed505bf4c9f04ddf98229b75
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Device Details

Leonardo Dual Laser System
TW: ๆŽๅฅง็ดๅคš้›™้ ป้›ทๅฐ„ๅ„€
Risk Class 2
MD

Registration Details

fc0db080ed505bf4c9f04ddf98229b75

Ministry of Health Medical Device Import No. 031921

DHA05603192107

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

Dec 10, 2018

Dec 10, 2023