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Crystallized fluorescence instrument for clinical use (unsterilized) - Taiwan Registration d0d6c5ec80c1b435f30c5f2fa1dcbf4d

Access comprehensive regulatory information for Crystallized fluorescence instrument for clinical use (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d0d6c5ec80c1b435f30c5f2fa1dcbf4d and manufactured by DiagnOptics Technologies B.V.. The authorized representative in Taiwan is JINGS INSTRUMENT CO., LTD..

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d0d6c5ec80c1b435f30c5f2fa1dcbf4d
Registration Details
Taiwan FDA Registration: d0d6c5ec80c1b435f30c5f2fa1dcbf4d
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Device Details

Crystallized fluorescence instrument for clinical use (unsterilized)
TW: ๆ™ถๅฏฆ ่‡จๅบŠไฝฟ็”จ็š„่žขๅ…‰ๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

d0d6c5ec80c1b435f30c5f2fa1dcbf4d

DHA084a0017901

Company Information

Netherlands

Product Details

Limited to the classification and grading management measures of medical equipment "fluorescence instrument for clinical use (A.2560)" the first level identification range.

A Clinical chemistry and clinical toxicology

A.2560 Fluorometer for clinical use

Dates and Status

May 17, 2023

Oct 31, 2025