Taiwan FDA registration d6ec891f01b1db608f3e5dc3e85dd829
"Kuken" heat shiki (unsterilized)
TW: “久保健”熱敷墊 (未滅菌)
Taiwan·Risk Class 1·SHIAN JIA MEEI ENTERPRISE CO., LTD.·Registered Sep 11, 2014 – Sep 11, 2024ExpiredRegistration details
- Analysis ID
- d6ec891f01b1db608f3e5dc3e85dd829
Company information
- Manufacturer
- SHIAN JIA MEEI ENTERPRISE CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- JEOU BAO JIANN HEALTH ENTERPRISE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the "Power Hot Compress Mat (O.5740)" of the Measures for the Classification and Grading of Medical Equipment.
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5740 動力式熱敷墊
- Import Information
- 委託製造;; 國產;; QMS/QSD
Dates and status
- Registration Date
- Sep 11, 2014
- Expiry Date
- Sep 11, 2024
About this record
Access comprehensive regulatory information for "Kuken" heat shiki (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d6ec891f01b1db608f3e5dc3e85dd829 and manufactured by SHIAN JIA MEEI ENTERPRISE CO., LTD.. The authorized representative in Taiwan is JEOU BAO JIANN HEALTH ENTERPRISE CO., LTD..
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