Taiwan FDA registration b10c70c41c6ad06e081581188a96c1ef

"Hede" platelet oscillator (unsterilized)

TW: “和德”血小板振盪器 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HOTECH INSTRUMENTS CORP.·Registered Jan 29, 2008 – Jan 29, 2023Cancelled
Registration details
Analysis ID
b10c70c41c6ad06e081581188a96c1ef
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
HOTECH INSTRUMENTS CORP.
Product details
Intended Use
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)".
Product Type (Level 1)
B Hematology, pathology, and genetics
Product Type (Level 2)
B.9195 Blood Mixers and Blood Gravimetric Analysis Devices
Import Information
QMS/QSD;; 國產
Dates and status
Registration Date
Jan 29, 2008
Expiry Date
Jan 29, 2023
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

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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