Taiwan FDA registration a05a9ec4b5fce662ce5a81bfdf14b116

"Kangyang" manual wheelchair

TW: “康揚”手動輪椅
Taiwan flagTaiwan·Risk Class 1·FOSHAN CITY NANHAI KAIYANG MEDICAL EQUIPMENT CO., LTD.·Registered Jul 17, 2007 – Jul 17, 2012Cancelled
Registration details
Analysis ID
a05a9ec4b5fce662ce5a81bfdf14b116
Customs Code
DHA04600040802
Company information
Manufacturer Country
China
Authorized Representative
KARMA MEDICAL PRODUCTS CO., LTD.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Mechanical Wheelchair (O.3850)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3850 Mechanical wheelchairs
Import Information
Chinese goods;; input
Dates and status
Registration Date
Jul 17, 2007
Expiry Date
Jul 17, 2012
Cancellation Date
Apr 09, 2014
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 "Kangyang" manual wheelchair in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a05a9ec4b5fce662ce5a81bfdf14b116 and manufactured by FOSHAN CITY NANHAI KAIYANG MEDICAL EQUIPMENT CO., LTD.. The authorized representative in Taiwan is KARMA MEDICAL PRODUCTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 5 companies making similar products including KARMA MEDICAL PRODUCTS CO., LTD., Changzhou ZhongHe Wheelchair Co., LTD., and 5 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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