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"Koster" Utyss system - Taiwan Registration f954bf8f546ef6ea1587ea4582e30628

Access comprehensive regulatory information for "Koster" Utyss system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f954bf8f546ef6ea1587ea4582e30628 and manufactured by KORUST Co., Ltd.. The authorized representative in Taiwan is DIAMOND BIOTECHNOLOGY 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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f954bf8f546ef6ea1587ea4582e30628
Registration Details
Taiwan FDA Registration: f954bf8f546ef6ea1587ea4582e30628
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Device Details

"Koster" Utyss system
TW: โ€œๅฏ‡ๆ–ฏ็‰นโ€ๅ„ชๆๆ–ฏ็ณป็ตฑ
Risk Class 2

Registration Details

f954bf8f546ef6ea1587ea4582e30628

DHA05603164509

Company Information

Korea, Republic of

Product Details

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

I General, Plastic Surgery and Dermatology

I.4590 Focused Ultrasound Stimulator

Input;; The use of this device shall comply with the provisions of the Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing.

Dates and Status

Sep 27, 2018

Sep 27, 2028