Taiwan FDA registration 6fa74de39bd35ed0a96f5b8fadbf994d

"Medical technology" oxygen nasal cannula (unsterilized)

TW: "醫技"氧氣鼻管(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ZHEJIANG YUANTONG MEDICAL APPLIANCES CO., LTD·Registered Nov 14, 2018 – Nov 14, 2028Active
Registration details
Analysis ID
6fa74de39bd35ed0a96f5b8fadbf994d
Customs Code
DHA09600360502
Company information
Manufacturer Country
China
Authorized Representative
E-GMED HEALTH CO., LTD
Product details
Intended Use
Limited to the first level identification range of the "nasal oxygen cannula (D.5340)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5340 Nasal oxygen cannula
Import Information
Chinese goods;; input
Dates and status
Registration Date
Nov 14, 2018
Expiry Date
Nov 14, 2028
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About this record

Access comprehensive regulatory information for "Medical technology" oxygen nasal cannula (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6fa74de39bd35ed0a96f5b8fadbf994d 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, 3 companies making similar products including GCMEDICA ENTERPRISE LTD. (WUXI)'S, HANGZHOU YUANTONG MEDICAL APPLIANCE CO., LTD, and 3 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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