Taiwan FDA registration eacfd3f200f9dc1ba712d0daf93490d8

"Medtech" flow mask (unsterilized)

TW: "醫技"流量面罩(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ZHEJIANG YUANTONG MEDICAL APPLIANCES CO., LTD·Registered Nov 14, 2018 – Nov 14, 2023Expired
Registration details
Analysis ID
eacfd3f200f9dc1ba712d0daf93490d8
Customs Code
DHA09600360206
Company information
Manufacturer Country
China
Authorized Representative
E-GMED HEALTH CO., LTD
Product details
Intended Use
It is limited to the first level of identification scope of the "Venturi Face Mask (D.5600)" of the management method for the classification and grading of medical devices.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5600 Venturi面罩
Import Information
Chinese goods;; input
Dates and status
Registration Date
Nov 14, 2018
Expiry Date
Nov 14, 2023
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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 eacfd3f200f9dc1ba712d0daf93490d8 and manufactured by ZHEJIANG YUANTONG MEDICAL APPLIANCES 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 HANGZHOU YUANTONG MEDICAL APPLIANCE 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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