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"Meekek" non-invasive respiratory care system - Taiwan Registration a2bc2c0fd73cce04818f2b09a4a5289e

Access comprehensive regulatory information for "Meekek" non-invasive respiratory care system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a2bc2c0fd73cce04818f2b09a4a5289e and manufactured by MEKICS Co., Ltd.. The authorized representative in Taiwan is BROJAW 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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a2bc2c0fd73cce04818f2b09a4a5289e
Registration Details
Taiwan FDA Registration: a2bc2c0fd73cce04818f2b09a4a5289e
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Device Details

"Meekek" non-invasive respiratory care system
TW: โ€œ็พŽๅ‡ฑๅ…‹โ€ ้žไพตๅ…ฅๅผๅ‘ผๅธ็…ง้กง็ณป็ตฑ
Risk Class 2

Registration Details

a2bc2c0fd73cce04818f2b09a4a5289e

DHA05603501101

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

D Anesthesiology; E Cardiovascular Medicine Science

D.5905 ้ž้€ฃ็บŒๆ€งๅ‘ผๅธๅ™จ;; E.2700 ่ก€ๆฐง้ฃฝๅ’Œๆธฌๅฎšๅ„€

import

Dates and Status

Oct 28, 2021

Oct 28, 2026