Taiwan FDA registration f422597fa4848843473e7057c1f2e819
"min-jier" Capillary tube (Non-Sterile)
TW: "明傑"毛細血液收集管(未滅菌)
Taiwan·Risk Class 1·MD·VITREX MEDICAL A/S·Registered Jan 30, 2019 – Jan 30, 2024ExpiredRegistration details
- Analysis ID
- f422597fa4848843473e7057c1f2e819
- License Form
- Ministry of Health Medical Device Import No. 020083
- Customs Code
- DHA09402008302
Company information
- Manufacturer
- VITREX MEDICAL A/S
- Manufacturer Country
- Denmark
- Authorized Representative
- MIN JIER FIRM
Product details
- Intended Use
- Limited to the first level identification range of "Capillary Blood Collection Tube (B.6150)" under the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- B Hematology and pathology devices
- Product Type (Level 2)
- B6150 Capillary blood collection tube
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jan 30, 2019
- Expiry Date
- Jan 30, 2024
About this record
Access comprehensive regulatory information for "min-jier" Capillary tube (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 f422597fa4848843473e7057c1f2e819 and manufactured by VITREX MEDICAL A/S. The authorized representative in Taiwan is MIN JIER FIRM.
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