Taiwan FDA registration 4495e6437161ebfade209db7e0e44141

"Yi Sheng" tracheobronchial suction catheter (sterilized)

TW: "毅升" 氣管支氣管抽吸導管 (滅菌)
Taiwan flagTaiwan·Risk Class 1·Jiangsu Yaohua Medical Device Technology Co., Ltd.·Registered Mar 30, 2011 – Mar 30, 2021Cancelled
Registration details
Analysis ID
4495e6437161ebfade209db7e0e44141
Customs Code
DHA04600131401
Company information
Manufacturer Country
China
Authorized Representative
E-UP CO., LTD.
Product details
Intended Use
Limited to the management method of medical equipment, tracheobronchial suction catheter (D.6810) level 1 identification range.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.6810 Pneumatic bronchial suction guide tube
Import Information
Input;; QMS/QSD;; Chinese goods
Dates and status
Registration Date
Mar 30, 2011
Expiry Date
Mar 30, 2021
Cancellation Date
Sep 08, 2023
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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About this record

Access comprehensive regulatory information for "Yi Sheng" tracheobronchial suction catheter (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4495e6437161ebfade209db7e0e44141 and manufactured by Jiangsu Yaohua Medical Device Technology 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 INTEGRAL MEDICAL PRODUCTS 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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