Taiwan FDA registration ae04b4e95112c415396164e152212107

"Riester" Operating Headlamp (Non-Sterile)

TW: "雷伊斯特" 手術用頭燈 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUDOLF RIESTER GMBH·Registered May 18, 2015 – May 18, 2025Expired
Registration details
Analysis ID
ae04b4e95112c415396164e152212107
License Form
Ministry of Health Medical Device Import No. 015229
Customs Code
DHA09401522900
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 "Surgical Headlamps (M.4335)".
Product Type (Level 1)
M Ophthalmic devices
Product Type (Level 2)
M4335 Surgical headlamp
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" Operating Headlamp (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 ae04b4e95112c415396164e152212107 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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