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"Kaijie" automatic capillary electrophoresis instrument (unsterilized) - Taiwan Registration 485c70af81dfaace2486eb15450e46cf

Access comprehensive regulatory information for "Kaijie" automatic capillary electrophoresis instrument (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 485c70af81dfaace2486eb15450e46cf and manufactured by QIAGEN GMBH;; Zollner Electronics GmbH. The authorized representative in Taiwan is QIAGEN TAIWAN COMPANY LIMITED.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including QIAGEN 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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485c70af81dfaace2486eb15450e46cf
Registration Details
Taiwan FDA Registration: 485c70af81dfaace2486eb15450e46cf
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Device Details

"Kaijie" automatic capillary electrophoresis instrument (unsterilized)
TW: "ๅ‡ฑๆฐ" ๅ…จ่‡ชๅ‹•ๆฏ›็ดฐ็ฎก้›ปๆณณๅ„€ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

485c70af81dfaace2486eb15450e46cf

DHA084a0005203

Company Information

Germany;;Switzerland

Product Details

Limited to the first level identification range of "Electrophoresis Equipment for Clinical Use (A.2485)" of the Measures for the Classification and Grading Management of Medical Equipment.

A Clinical chemistry and clinical toxicology

A.2485 Electrophoresis equipment for clinical use

Dates and Status

Apr 12, 2022

Oct 31, 2024

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