"Fisher" Spectrophotometer for Clinical Use (Unsterilized)
- Analysis ID
- 35ebfe17009a716dc90608cb8293d4f9
- Customs Code
- DHA09401446800
- Manufacturer
- FISCHER ANALYSEN INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PRINCETON INTERNATIONAL INDUSTRIES TAIWAN CORP.
- 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
- Registration Date
- Aug 29, 2014
- Expiry Date
- Aug 29, 2024
- Cancellation Date
- Sep 30, 2021
- Status
- Logged out
- Reason
- 轉為登錄字號
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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.