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"Keeler" Magnifying Loupes and accessories (Non-Sterile) - Taiwan Registration 2cf907587d4a2bbcc3b19e233a0dbb02

Access comprehensive regulatory information for "Keeler" Magnifying Loupes and accessories (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 2cf907587d4a2bbcc3b19e233a0dbb02 and manufactured by Keeler Limited. The authorized representative in Taiwan is TAIWAN INSTRUMENT 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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2cf907587d4a2bbcc3b19e233a0dbb02
Registration Details
Taiwan FDA Registration: 2cf907587d4a2bbcc3b19e233a0dbb02
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Device Details

"Keeler" Magnifying Loupes and accessories (Non-Sterile)
TW: "ๅ‡ฑๅ‹’" ๆ”พๅคง้กๅŠๅ…ถ้™„ไปถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2cf907587d4a2bbcc3b19e233a0dbb02

Ministry of Health Medical Device Import No. 021447

DHA09402144706

Company Information

United Kingdom

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Apr 10, 2020

Apr 10, 2025