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"Riester" Operating Headlamp (Non-Sterile) - Taiwan Registration bb01e20cda24a11f0792c26c62660652

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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bb01e20cda24a11f0792c26c62660652
Registration Details
Taiwan FDA Registration: bb01e20cda24a11f0792c26c62660652
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Device Details

"Riester" Operating Headlamp (Non-Sterile)
TW: "็‘žๅธ"ๆ‰‹่ก“็”จ้ ญ็‡ˆ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

bb01e20cda24a11f0792c26c62660652

Ministry of Health Medical Device Import No. 014005

DHA09401400509

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

Apr 01, 2014

Apr 01, 2024

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