Taiwan FDA registration dc0d8d4cf4ba7354773267232aedc7a8

"Aon" endotracheal probe (unsterilized) 

TW: "怡安" 氣管內管探針 (未滅菌) 
Taiwan flagTaiwan·Risk Class 1·HANGZHOU SHANYOU MEDICAL EQUIPMENT CO., LTD·Registered Mar 22, 2011 – Mar 22, 2016Cancelled
Registration details
Analysis ID
dc0d8d4cf4ba7354773267232aedc7a8
Customs Code
DHA04600130500
Company information
Manufacturer Country
China
Authorized Representative
LILY MEDICAL CORPORATION
Product details
Intended Use
Limited to the first level recognition range of endotracheal tube probe (D.5790) of the management method for medical equipment.
Product Type (Level 1)
D Anesthesiology
Product Type (Level 2)
D.5790 氣管內管探針
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Mar 22, 2011
Expiry Date
Mar 22, 2016
Cancellation Date
May 28, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Aon" endotracheal probe (unsterilized)  in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dc0d8d4cf4ba7354773267232aedc7a8 and manufactured by HANGZHOU SHANYOU MEDICAL EQUIPMENT 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 LILY MEDICAL CORPORATION, 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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