Taiwan FDA registration ac8f15f22b17dc70e264e7bfbbf357c1

"Medtech" flow mask (unsterilized)

TW: "醫技"流量面罩(未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANGZHOU YUANTONG MEDICAL APPLIANCE CO., LTD·Registered Aug 04, 2011 – Aug 04, 2021Cancelled
Registration details
Analysis ID
ac8f15f22b17dc70e264e7bfbbf357c1
Customs Code
DHA04600142609
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
import
Dates and status
Registration Date
Aug 04, 2011
Expiry Date
Aug 04, 2021
Cancellation Date
Aug 15, 2023
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 ac8f15f22b17dc70e264e7bfbbf357c1 and manufactured by HANGZHOU YUANTONG MEDICAL APPLIANCE CO., LTD. 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 ZHEJIANG YUANTONG MEDICAL APPLIANCES CO., LTD, GCMEDICA ENTERPRISE LTD. (WUXI)'S, 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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