Taiwan FDA registration 9855418cbeb9b83eebc9546d27356934
"Remel" Microorganism differentiation and identification device (Non-Sterile)
TW: "銳邁" 微生物鑑別及測定器材 (未滅菌)
Taiwan·Risk Class 1·MD·REMEL EUROPE LIMITED·Registered Jun 03, 2019 – Jun 03, 2024ExpiredRegistration details
- Analysis ID
- 9855418cbeb9b83eebc9546d27356934
- License Form
- Ministry of Health Medical Device Import No. 020515
- Customs Code
- DHA09402051505
Company information
- Manufacturer
- REMEL EUROPE LIMITED
- Manufacturer Country
- United Kingdom
- Authorized Representative
- CREATIVE LIFE SCIENCE CO., LTD.
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Microbial Identification and Measurement Equipment (C.2660)".
- Product Type (Level 1)
- C Immunology and microbiology devices
- Product Type (Level 2)
- C2660 Microbial identification and assay equipment
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jun 03, 2019
- Expiry Date
- Jun 03, 2024
About this record
Access comprehensive regulatory information for "Remel" Microorganism differentiation and identification 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 9855418cbeb9b83eebc9546d27356934 and manufactured by REMEL EUROPE LIMITED. The authorized representative in Taiwan is CREATIVE LIFE SCIENCE CO., LTD..
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