Taiwan FDA registration 87166440ab26aa1b0370509d9ad6b11a

"Escent" airway connector (unsterilized)

TW: "毅升" 氣道連接器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANGZHOU SUPERDS INDUSTRY CO., LTD·Registered Aug 27, 2018 – Aug 27, 2028Active
Registration details
Analysis ID
87166440ab26aa1b0370509d9ad6b11a
Customs Code
DHA09600353800
Company information
Manufacturer Country
China
Authorized Representative
E-UP CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Airway Connector (D.5810)" of the Administrative Measures for the Classification and Grading of Medical Devices.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5810 Airway connectors
Import Information
Chinese goods;; input
Dates and status
Registration Date
Aug 27, 2018
Expiry Date
Aug 27, 2028
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About this record

Access comprehensive regulatory information for "Escent" airway connector (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87166440ab26aa1b0370509d9ad6b11a and manufactured by HANGZHOU SUPERDS INDUSTRY CO., LTD. The authorized representative in Taiwan is E-UP CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including NINGBO SHENGYURUI MEDICAL APPLIANCE CO., LTD., and 1 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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