Taiwan FDA registration 88f3595bb24715a0106dc8fc0d70b9bc
"Fischer" Microbiological Specimen Collection and Transport Device (Non-Sterile)
TW: "費雪" 微生物樣本收集及輸送器材 (未滅菌)
Taiwan·Risk Class 1·MD·FISCHER ANALYSEN INSTRUMENTE GMBH·Registered Feb 13, 2020 – Feb 13, 2025ExpiredRegistration details
- Analysis ID
- 88f3595bb24715a0106dc8fc0d70b9bc
- License Form
- Ministry of Health Medical Device Import No. 021261
- Customs Code
- DHA09402126105
Company information
- Manufacturer
- FISCHER ANALYSEN INSTRUMENTE GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- HOPE WANG ENTERPRISES CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Sample Collection and Delivery Equipment (C.2900)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2900 Microbial sample collection and delivery device
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 13, 2020
- Expiry Date
- Feb 13, 2025
About this record
Access comprehensive regulatory information for "Fischer" Microbiological Specimen Collection and Transport Device (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 88f3595bb24715a0106dc8fc0d70b9bc and manufactured by FISCHER ANALYSEN INSTRUMENTE GMBH. The authorized representative in Taiwan is HOPE WANG ENTERPRISES CO., LTD..
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