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"Meroji" Aiba's diathermy device - Taiwan Registration 899b0f50a50d99cd48252941a36a4d4a

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..

This page provides complete technical specifications, regulatory compliance details. 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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899b0f50a50d99cd48252941a36a4d4a
Registration Details
Taiwan FDA Registration: 899b0f50a50d99cd48252941a36a4d4a
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Device Details

"Meroji" Aiba's diathermy device
TW: โ€œ็พŽ็พ…ๅ‰โ€ ๆ„›ๅทด้€็†ฑๆฒป็™‚ๅ„€
Risk Class 3

Registration Details

899b0f50a50d99cd48252941a36a4d4a

DHA05603501904

Company Information

Italy

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.9999 Miscellaneous

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

Nov 04, 2021

Nov 04, 2026