Taiwan FDA registration a567abadebbde07c65fcc9ab9d8ed391

"Medtech" flow mask (unsterilized)

TW: "醫技"流量面罩(未滅菌)
Taiwan flagTaiwan·Risk Class 1·GCMEDICA ENTERPRISE LTD. (WUXI)'S·Registered Mar 25, 2013 – Mar 25, 2018Cancelled
Registration details
Analysis ID
a567abadebbde07c65fcc9ab9d8ed391
Customs Code
DHA04600186407
Company information
Manufacturer Country
China
Authorized Representative
E-GMED HEALTH CO., LTD
Product details
Intended Use
Limited to the first level recognition range of the Venturi mask (D.5600) of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5600 Venturi面罩
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Mar 25, 2013
Expiry Date
Mar 25, 2018
Cancellation Date
Nov 20, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Medtech" flow mask (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a567abadebbde07c65fcc9ab9d8ed391 and manufactured by GCMEDICA ENTERPRISE LTD. (WUXI)'S. The authorized representative in Taiwan is E-GMED HEALTH CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including HANGZHOU YUANTONG MEDICAL APPLIANCE CO., LTD, ZHEJIANG YUANTONG MEDICAL APPLIANCES CO., LTD, and 2 recent registrations in the same category. 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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