Taiwan FDA registration 18b1ba99f97dd78635d9a71d551cb653

"Fisher" Spectrophotometer for Clinical Use (Unsterilized)

TW: "菲雪" 臨床使用的分光光度計 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·FISCHER ANALYSEN INSTRUMENTE GMBH·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
18b1ba99f97dd78635d9a71d551cb653
Customs Code
DHA08401446801
Company information
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level identification range of the Measures for the Classification and Grading of Medical Devices "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)".
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2300 Colorimeter, photometer, or spectrophotometer for clinical use
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "Fisher" Spectrophotometer 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 18b1ba99f97dd78635d9a71d551cb653 and manufactured by FISCHER ANALYSEN INSTRUMENTE GMBH. The authorized representative in Taiwan is PRINCETON INTERNATIONAL INDUSTRIES TAIWAN CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including FISCHER ANALYSEN INSTRUMENTE 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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