Taiwan FDA registration 17fc2a735cdb50f1b83d6db3f98f9d47

"Changfeng" hot and cold compress pad (unsterilized)

TW: “昌豐” 冷熱敷墊 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Taiwan Shujie Co., Ltd. Triple Factory·Registered Apr 06, 2021 – Apr 06, 2026Cancelled
Registration details
Analysis ID
17fc2a735cdb50f1b83d6db3f98f9d47
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
SUNLUS CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5700 醫療用冷熱敷裝置
Import Information
Contract manufacturing;; Domestic
Dates and status
Registration Date
Apr 06, 2021
Expiry Date
Apr 06, 2026
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for "Changfeng" hot and cold compress pad (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 17fc2a735cdb50f1b83d6db3f98f9d47 and manufactured by Taiwan Shujie Co., Ltd. Triple Factory. The authorized representative in Taiwan is SUNLUS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Taiwan Shujie Co., Ltd. Triple Factory;; Changfeng International Co., Ltd, R&R MEDICAL CORPORATION 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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