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"Riester" Operating Headlamp (Non-Sterile) - Taiwan Registration ae04b4e95112c415396164e152212107

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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ae04b4e95112c415396164e152212107
Registration Details
Taiwan FDA Registration: ae04b4e95112c415396164e152212107
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Device Details

"Riester" Operating Headlamp (Non-Sterile)
TW: "้›ทไผŠๆ–ฏ็‰น" ๆ‰‹่ก“็”จ้ ญ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ae04b4e95112c415396164e152212107

Ministry of Health Medical Device Import No. 015229

DHA09401522900

Company Information

Germany

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Surgical Headlamps (M.4335)".

M Ophthalmic devices

M4335 Surgical headlamp

Imported from abroad

Dates and Status

May 18, 2015

May 18, 2025

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