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"Hede" platelet oscillator (unsterilized) - Taiwan Registration b10c70c41c6ad06e081581188a96c1ef

Access comprehensive regulatory information for "Hede" platelet oscillator (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b10c70c41c6ad06e081581188a96c1ef and manufactured by HOTECH INSTRUMENTS CORP.. The authorized representative in Taiwan is HOTECH INSTRUMENTS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOTECH INSTRUMENTS CORP., 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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b10c70c41c6ad06e081581188a96c1ef
Registration Details
Taiwan FDA Registration: b10c70c41c6ad06e081581188a96c1ef
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Device Details

"Hede" platelet oscillator (unsterilized)
TW: โ€œๅ’Œๅพทโ€่ก€ๅฐๆฟๆŒฏ็›ชๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

b10c70c41c6ad06e081581188a96c1ef

Company Information

Taiwan, Province of China

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Blood Mixers and Blood Gravimetric Analysis Devices (B.9195)".

B Hematology, pathology, and genetics

B.9195 Blood Mixers and Blood Gravimetric Analysis Devices

QMS/QSD;; ๅœ‹็”ข

Dates and Status

Jan 29, 2008

Jan 29, 2023

Sep 30, 2021

Cancellation Information

Logged out

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