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"Vorotek" Operating Headlamp (Non-Sterile) - Taiwan Registration b91895077a6c0287b8b8ca7221866ff0

Access comprehensive regulatory information for "Vorotek" 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 b91895077a6c0287b8b8ca7221866ff0 and manufactured by VOROTEK PTY LTD. The authorized representative in Taiwan is JAG MEDICAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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b91895077a6c0287b8b8ca7221866ff0
Registration Details
Taiwan FDA Registration: b91895077a6c0287b8b8ca7221866ff0
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Device Details

"Vorotek" Operating Headlamp (Non-Sterile)
TW: "ไฝ›็พ…ๆๅ…‹" ๆ‰‹่ก“็”จ้ ญ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b91895077a6c0287b8b8ca7221866ff0

Ministry of Health Medical Device Import No. 016483

DHA09401648303

Company Information

Australia

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 03, 2016

May 03, 2021