Taiwan FDA registration 893b5d6b70c8205351cb854205d68edd
"Fischer" Spectrophotometer for clinical use (Non-sterile)
TW: "菲雪" 臨床使用的分光光度計 (未滅菌)
Taiwan·Risk Class 1·MD·FISCHER ANALYSEN INSTRUMENTE GMBH·Registered Oct 27, 2021 – Oct 31, 2022CancelledRegistration details
- Analysis ID
- 893b5d6b70c8205351cb854205d68edd
- License Form
- Ministry of Health Medical Device Import Registration No. a00008
- Customs Code
- DHA084a0000800
Company information
- Manufacturer
- FISCHER ANALYSEN INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- PRINCETON INTERNATIONAL INDUSTRIES TAIWAN CORP.
Product details
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2300 Colorimeter, photometer, or spectrophotometer for clinical use
Dates and status
- Registration Date
- Oct 27, 2021
- Expiry Date
- Oct 31, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for "Fischer" Spectrophotometer for clinical use (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 893b5d6b70c8205351cb854205d68edd and manufactured by FISCHER ANALYSEN INSTRUMENTE GMBH. The authorized representative in Taiwan is PRINCETON INTERNATIONAL INDUSTRIES TAIWAN CORP..
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