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"Kangyang" manual wheelchair - Taiwan Registration 768f802db579cc65064c5a7d26ca1b4b

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 768f802db579cc65064c5a7d26ca1b4b and manufactured by KARMA MEDICAL PRODUCTS 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., FOSHAN CITY NANHAI KAIYANG MEDICAL EQUIPMENT 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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768f802db579cc65064c5a7d26ca1b4b
Registration Details
Taiwan FDA Registration: 768f802db579cc65064c5a7d26ca1b4b
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Device Details

"Kangyang" manual wheelchair
TW: "ๅบทๆš" ๆ‰‹ๅ‹•่ผชๆค…
Risk Class 1
Cancelled

Registration Details

768f802db579cc65064c5a7d26ca1b4b

DHY04300010503

Company Information

Taiwan, Province of China

Product Details

A wheeled manual device for medical use, which can be used when the movement of patients who are restricted to a sitting position.

o Physical Medical Sciences

Domestic

Dates and Status

Jul 21, 2005

Jul 21, 2010

Nov 15, 2012

Cancellation Information

Logged out

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