Taiwan FDA registration 899b0f50a50d99cd48252941a36a4d4a
"Meroji" Aiba's diathermy device
TW: “美羅吉” 愛巴透熱治療儀
Taiwan·Risk Class 3·MED-LOGIX S.r.l.·Registered Nov 04, 2021 – Nov 04, 2026ActiveRegistration details
- Analysis ID
- 899b0f50a50d99cd48252941a36a4d4a
- Customs Code
- DHA05603501904
Company information
- Manufacturer
- MED-LOGIX S.r.l.
- Manufacturer Country
- Italy
- Authorized Representative
- ANDERSON MEDICAL SUPPLY CO., LTD.
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.9999 Miscellaneous
- Import Information
- The use of this device shall comply with the provisions of the "Administrative Measures for the Implementation or Use of Medical Devices for Specific Medical Technology Inspection and Testing". input
Dates and status
- Registration Date
- Nov 04, 2021
- Expiry Date
- Nov 04, 2026
About this record
Access comprehensive regulatory information for "Meroji" Aiba's diathermy device in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number 899b0f50a50d99cd48252941a36a4d4a and manufactured by MED-LOGIX S.r.l.. The authorized representative in Taiwan is ANDERSON MEDICAL SUPPLY CO., LTD..
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