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"Kangyang" manual wheelchair - Taiwan Registration a05a9ec4b5fce662ce5a81bfdf14b116

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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a05a9ec4b5fce662ce5a81bfdf14b116
Registration Details
Taiwan FDA Registration: a05a9ec4b5fce662ce5a81bfdf14b116
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Device Details

"Kangyang" manual wheelchair
TW: โ€œๅบทๆšโ€ๆ‰‹ๅ‹•่ผชๆค…
Risk Class 1
Cancelled

Registration Details

a05a9ec4b5fce662ce5a81bfdf14b116

DHA04600040802

Company Information

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Mechanical Wheelchair (O.3850)".

o Physical Medical Sciences

O.3850 Mechanical wheelchairs

Chinese goods;; input

Dates and Status

Jul 17, 2007

Jul 17, 2012

Apr 09, 2014

Cancellation Information

Logged out

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