Taiwan FDA registration bb01e20cda24a11f0792c26c62660652

"Riester" Operating Headlamp (Non-Sterile)

TW: "瑞司"手術用頭燈(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·RUDOLF RIESTER GMBH·Registered Apr 01, 2014 – Apr 01, 2024Expired
Registration details
Analysis ID
bb01e20cda24a11f0792c26c62660652
License Form
Ministry of Health Medical Device Import No. 014005
Customs Code
DHA09401400509
Company information
Manufacturer Country
Germany
Authorized Representative
BOYANG MEDICAL TECHNOLOGY 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
Apr 01, 2014
Expiry Date
Apr 01, 2024
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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 bb01e20cda24a11f0792c26c62660652 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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