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"MEDIANA" Otoscope (Non-Sterile) - Taiwan Registration 4fc2c1060ca414cb3c1e4549dc0c3247

Access comprehensive regulatory information for "MEDIANA" Otoscope (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4fc2c1060ca414cb3c1e4549dc0c3247 and manufactured by MEDIANA CO., LTD.. The authorized representative in Taiwan is WHOLE WELL 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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4fc2c1060ca414cb3c1e4549dc0c3247
Registration Details
Taiwan FDA Registration: 4fc2c1060ca414cb3c1e4549dc0c3247
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Device Details

"MEDIANA" Otoscope (Non-Sterile)
TW: "็พŽๅธ้‚ฃ" ่€ณ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

4fc2c1060ca414cb3c1e4549dc0c3247

Ministry of Health Medical Device Import No. 020495

DHA09402049502

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".

G ENT device

G4770 Otoscope

Imported from abroad

Dates and Status

May 28, 2019

May 28, 2024