Taiwan FDA registration 35ebfe17009a716dc90608cb8293d4f9

"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 Aug 29, 2014 – Aug 29, 2024Cancelled
Registration details
Analysis ID
35ebfe17009a716dc90608cb8293d4f9
Customs Code
DHA09401446800
Company information
Manufacturer Country
Germany
Product details
Intended Use
Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.
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
Aug 29, 2014
Expiry Date
Aug 29, 2024
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 "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 35ebfe17009a716dc90608cb8293d4f9 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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