Taiwan FDA registration a2bc2c0fd73cce04818f2b09a4a5289e
"Meekek" non-invasive respiratory care system
TW: “美凱克” 非侵入式呼吸照顧系統
Registration details
- Analysis ID
- a2bc2c0fd73cce04818f2b09a4a5289e
- Customs Code
- DHA05603501101
Company information
- Manufacturer
- MEKICS Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BROJAW INC.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology; E Cardiovascular Medicine Science
- Product Type (Level 2)
- D.5905 非連續性呼吸器;; E.2700 血氧飽和測定儀
- Import Information
- import
Dates and status
- Registration Date
- Oct 28, 2021
- Expiry Date
- Oct 28, 2026
About this record
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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