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"Keeler" Operating Headlamp (Non-Sterile) - Taiwan Registration ce36f17c6884db23b30ef5864e5c75d3

Access comprehensive regulatory information for "Keeler" 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 ce36f17c6884db23b30ef5864e5c75d3 and manufactured by Keeler Limited. The authorized representative in Taiwan is TAIWAN INSTRUMENT CO., LTD..

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ce36f17c6884db23b30ef5864e5c75d3
Registration Details
Taiwan FDA Registration: ce36f17c6884db23b30ef5864e5c75d3
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Device Details

"Keeler" Operating Headlamp (Non-Sterile)
TW: "ๅ‡ฑๅ‹’" ๆ‰‹่ก“็”จ้ ญ็‡ˆ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ce36f17c6884db23b30ef5864e5c75d3

Ministry of Health Medical Device Import No. 021479

DHA09402147906

Company Information

United Kingdom

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 21, 2020

Apr 21, 2025