Pure Global

"Asquebian" Kudjoplas Laser - Taiwan Registration 52cf95e58086a59f16a348efe46cc424

Access comprehensive regulatory information for "Asquebian" Kudjoplas Laser in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 52cf95e58086a59f16a348efe46cc424 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
52cf95e58086a59f16a348efe46cc424
Registration Details
Taiwan FDA Registration: 52cf95e58086a59f16a348efe46cc424
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"Asquebian" Kudjoplas Laser
TW: โ€œ้˜ฟๆ–ฏๅ…‹ๆฏ”ๆฉโ€ๅบซๅ“ๆ™ฎๆ‹‰ๆ–ฏ้›ทๅฐ„ๅ„€
Risk Class 2
Cancelled

Registration Details

52cf95e58086a59f16a348efe46cc424

DHA00602287200

Company Information

Product Details

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

I General, Plastic Surgery and Dermatology

I.4810 Lasers for general surgical, orthopaedic and dermatological use

import

Dates and Status

Sep 30, 2011

Sep 30, 2016

Jun 28, 2018

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ