Taiwan FDA registration d7fb044b9c16e7f2e636d0133b79729a

Regal & Reishang Automatic Analyzer (Unsterilized)

TW: 禮雅尚 全自動分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·DIASORIN DEUTSCHLAND GMBH·Registered Mar 01, 2017 – Mar 01, 2022Cancelled
Registration details
Analysis ID
d7fb044b9c16e7f2e636d0133b79729a
Customs Code
DHA09401753402
Company information
Manufacturer Country
Germany
Authorized Representative
MEDRICH INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2160 Individual Photometric Chemistry Analyzer for Clinical Use
Import Information
Input;; QMS/QSD
Dates and status
Registration Date
Mar 01, 2017
Expiry Date
Mar 01, 2022
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 Regal & Reishang Automatic Analyzer (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d7fb044b9c16e7f2e636d0133b79729a and manufactured by DIASORIN DEUTSCHLAND GMBH. The authorized representative in Taiwan is MEDRICH INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DIASORIN DEUTSCHLAND 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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