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"Seton" Puferno laser system - Taiwan Registration 2cd81bed5fe64fee3cbe02c6d762ae2d

Access comprehensive regulatory information for "Seton" Puferno 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 2cd81bed5fe64fee3cbe02c6d762ae2d and manufactured by SCITON, INC.. The authorized representative in Taiwan is DYNAMIC MEDICAL TECHNOLOGIES INC..

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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2cd81bed5fe64fee3cbe02c6d762ae2d
Registration Details
Taiwan FDA Registration: 2cd81bed5fe64fee3cbe02c6d762ae2d
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Device Details

"Seton" Puferno laser system
TW: โ€œ่ณฝ้ “โ€ๆ™ฎ่ฒป่ซพ้›ทๅฐ„็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

2cd81bed5fe64fee3cbe02c6d762ae2d

DHA00601910400

Company Information

United States

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

Jul 10, 2008

Jul 10, 2018

Jun 07, 2022

Cancellation Information

Logged out

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