Taiwan FDA registration 00ef2fa4c6029152a9da3104460f9043

"Riester" Otoscope (Non-Sterile)

TW: "雷伊斯特" 耳鏡 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUDOLF RIESTER GMBH·Registered May 18, 2015 – May 18, 2025Expired
Registration details
Analysis ID
00ef2fa4c6029152a9da3104460f9043
License Form
Ministry of Health Medical Device Import No. 015230
Customs Code
DHA09401523008
Company information
Manufacturer Country
Germany
Authorized Representative
JUN FENG OPTICAL CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Otoscope (G.4770)".
Product Type (Level 1)
G ENT device
Product Type (Level 2)
G4770 Otoscope
Import Information
Imported from abroad
Dates and status
Registration Date
May 18, 2015
Expiry Date
May 18, 2025
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About this record

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 00ef2fa4c6029152a9da3104460f9043 and manufactured by RUDOLF RIESTER GMBH. The authorized representative in Taiwan is JUN FENG OPTICAL 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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