Taiwan FDA registration 1f80cd9b42e02c937da8c4239a6df25b

"Khanma" warm chamber (unsterilized)

TW: "汗馬" 溫熱艙 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Jul 25, 2016 – Jul 25, 2026Cancelled
Registration details
Analysis ID
1f80cd9b42e02c937da8c4239a6df25b
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
SHIAN JIA MEEI ENTERPRISE CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Power Thermal Cushion (O.5740)".
Product Type (Level 1)
o Physical Medical Sciences
Product Type (Level 2)
O.5740 動力式熱敷墊
Import Information
國產;; QMS/QSD
Dates and status
Registration Date
Jul 25, 2016
Expiry Date
Jul 25, 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 "Khanma" warm chamber (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 1f80cd9b42e02c937da8c4239a6df25b and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is SHIAN JIA MEEI ENTERPRISE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SHIAN JIA MEEI ENTERPRISE CO., LTD., 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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