Taiwan FDA registration f9b612e2e3bccac442488d030730df40

"Aon" tracheobronchial suction catheter (sterilized)

TW: “怡安”氣管支氣管抽吸導管 (滅菌)
Taiwan flagTaiwan·Risk Class 1·ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.·Registered Jun 16, 2009 – Jun 16, 2019Cancelled
Registration details
Analysis ID
f9b612e2e3bccac442488d030730df40
Customs Code
DHA04600073109
Company information
Manufacturer Country
China
Authorized Representative
LILY MEDICAL CORPORATION
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
Chinese goods;; Input;; QMS/QSD
Dates and status
Registration Date
Jun 16, 2009
Expiry Date
Jun 16, 2019
Cancellation Date
May 19, 2022
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Aon" 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 f9b612e2e3bccac442488d030730df40 and manufactured by ZHANGJIAGANG SHENGANG MEDICAL PRODUCTS CO., LTD.. The authorized representative in Taiwan is LILY MEDICAL CORPORATION.

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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