Taiwan FDA registration cd06ca3b10980031ce6e9fe0d9985787

"Jianpeng" mechanical wheelchair (unsterilized)

TW: "建鵬" 機械式輪椅 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY (LTD.)·Registered Sep 11, 2014 – Sep 11, 2019Cancelled
Registration details
Analysis ID
cd06ca3b10980031ce6e9fe0d9985787
Customs Code
DHA09600221701
Company information
Manufacturer Country
China
Authorized Representative
J. P. 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
Sep 11, 2014
Expiry Date
Sep 11, 2019
Cancellation Date
Jun 07, 2022
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 "Jianpeng" mechanical wheelchair (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cd06ca3b10980031ce6e9fe0d9985787 and manufactured by FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY (LTD.). The authorized representative in Taiwan is J. P. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including FOSHAN SHUNDE JOIN HARDWARE ENTERPRISE CO., LTD., FOSHAN DONGFANG MEDICAL EQUIPMENT MANUFACTORY(LTD.), and 2 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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