Taiwan FDA registration a80261b978e3dc08c13ed1028c878e5c

"Reais" hot and cold compress (unsterilized)

TW: “瑞艾”冷熱敷墊(未滅菌)
Taiwan flagTaiwan·Risk Class 1·DANYANG RAPID AID HOT AND COLD THERAPY PRODUCTS CO., LTD.;; RAPID AID CORP.·Registered Apr 22, 2021 – Apr 22, 2026Cancelled
Registration details
Analysis ID
a80261b978e3dc08c13ed1028c878e5c
Customs Code
DHA09600449701
Company information
Manufacturer Country
Canada;;China
Authorized Representative
Mingyo Global Inc.
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
QMS/QSD;; 輸入
Dates and status
Registration Date
Apr 22, 2021
Expiry Date
Apr 22, 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 "Reais" hot and cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a80261b978e3dc08c13ed1028c878e5c and manufactured by DANYANG RAPID AID HOT AND COLD THERAPY PRODUCTS CO., LTD.;; RAPID AID CORP.. The authorized representative in Taiwan is Mingyo Global Inc..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DANYANG RAPID AID HOT AND COLD THERAPY PRODUCTS CO., LTD.;; RAPID AID CORP., 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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