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"Asquebien" Kudrow Laser - Taiwan Registration b86d9f7a1b6f431a355915ad6f6f07ea

Access comprehensive regulatory information for "Asquebien" Kudrow Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number b86d9f7a1b6f431a355915ad6f6f07ea and manufactured by ASCLEPION LASER TECHNOLOGIES GMBH. The authorized representative in Taiwan is COLLAMATRIX 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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b86d9f7a1b6f431a355915ad6f6f07ea
Registration Details
Taiwan FDA Registration: b86d9f7a1b6f431a355915ad6f6f07ea
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Device Details

"Asquebien" Kudrow Laser
TW: "้˜ฟๆ–ฏๅ…‹ๆฏ”ๆฉ" ๅบซๅ“้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

b86d9f7a1b6f431a355915ad6f6f07ea

DHA00601202801

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

import

Dates and Status

Sep 21, 2005

Sep 21, 2020

Jun 22, 2022

Cancellation Information

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