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"Riester" Otoscope (Non-Sterile) - Taiwan Registration 7e1c114ca85674d4fe96541f28fbb8e0

Access comprehensive regulatory information for "Riester" 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 7e1c114ca85674d4fe96541f28fbb8e0 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is BOYANG MEDICAL TECHNOLOGY CO., LTD.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including RUDOLF RIESTER GMBH, 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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7e1c114ca85674d4fe96541f28fbb8e0
Registration Details
Taiwan FDA Registration: 7e1c114ca85674d4fe96541f28fbb8e0
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Device Details

"Riester" Otoscope (Non-Sterile)
TW: "็‘žๅธ"่€ณ้ก(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7e1c114ca85674d4fe96541f28fbb8e0

Ministry of Health Medical Device Import No. 014004

DHA09401400407

Company Information

Germany

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

Apr 01, 2014

Apr 01, 2024

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