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“Asclepion” MeDioStar laser - Taiwan Registration 8096cc6afbb8c9e4c71dd803e9d20c0e

Access comprehensive regulatory information for “Asclepion” MeDioStar laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 8096cc6afbb8c9e4c71dd803e9d20c0e and manufactured by Asclepion Laser Technologies GmbH. The authorized representative in Taiwan is QUALTECH CONSULTING 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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8096cc6afbb8c9e4c71dd803e9d20c0e
Registration Details
Taiwan FDA Registration: 8096cc6afbb8c9e4c71dd803e9d20c0e
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Device Details

“Asclepion” MeDioStar laser
TW: “阿斯克比恩”密迪歐星雷射儀
Risk Class 2
MD

Registration Details

8096cc6afbb8c9e4c71dd803e9d20c0e

Ministry of Health Medical Device Import No. 034407

DHA05603440708

Company Information

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

Mar 21, 2021

Mar 21, 2026