Taiwan FDA registration e660a5d974cf3d615f5bf9dd7b56fe39

"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·INTEGRAL MEDICAL PRODUCTS CO., LTD.·Registered Dec 22, 2010 – Dec 22, 2015Cancelled
Registration details
Analysis ID
e660a5d974cf3d615f5bf9dd7b56fe39
Customs Code
DHA04600120901
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;; Chinese goods;; QMS/QSD
Dates and status
Registration Date
Dec 22, 2010
Expiry Date
Dec 22, 2015
Cancellation Date
Aug 09, 2018
Cancellation information
Status
Logged out
Reason
未展延而逾期者;;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 e660a5d974cf3d615f5bf9dd7b56fe39 and manufactured by INTEGRAL MEDICAL PRODUCTS 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 Jiangsu Yaohua Medical Device Technology 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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