Taiwan FDA registration 9994cb4a2ad0ec5a56e00edffd36ef62

"Kaiyang Technology" torso device (unsterilized)

TW: “開陽科技”軀幹裝具 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Kaiyang Technology Co., Ltd.;; Xinshifa Enterprise Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2025Cancelled
Registration details
Analysis ID
9994cb4a2ad0ec5a56e00edffd36ef62
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MIZAR Co., Ltd.
Product details
Intended Use
Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Torso Equipment (O.3490)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.3490 Torso mounting
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
Cancellation Date
Jul 28, 2023
Cancellation information
Status
Logged out
Reason
自行鍵入
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About this record

Access comprehensive regulatory information for "Kaiyang Technology" torso device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9994cb4a2ad0ec5a56e00edffd36ef62 and manufactured by Kaiyang Technology Co., Ltd.;; Xinshifa Enterprise Co., Ltd. The authorized representative in Taiwan is MIZAR Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SIN SHI FA ENTERPRISE LIMITED, 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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