Taiwan FDA registration 3e1025bec2316076005b05453623f1c9
Kabon Automated Sample Preparation System (Unsterilized)
TW: 卡邦全自動樣品製備系統(未滅菌)
Registration details
- Analysis ID
- 3e1025bec2316076005b05453623f1c9
- Customs Code
- DHA09402256402
Company information
- Manufacturer
- COPAN WASP S.R.L.
- Manufacturer Country
- Italy
- Authorized Representative
- PAN ASIA BIOMEDICAL TECHNOLOGY INC.
Product details
- Intended Use
- Limited to the classification and grading management of medical devices, "turbidimetric meter for clinical use (A.2700)" and "microtitration dilution and dispensing device (C.2500)" level 1 identification range.
- Product Type (Level 1)
- A Clinical Chemistry and Clinical Toxicology;; C Immunology and Microbiology
- Product Type (Level 2)
- A.2700 臨床使用的比濁計;; C.2500 微滴定稀釋及分配器材
- Import Information
- Input;; QMS/QSD
Dates and status
- Registration Date
- May 20, 2021
- Expiry Date
- May 20, 2026
About this record
Access comprehensive regulatory information for Kabon Automated Sample Preparation System (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 3e1025bec2316076005b05453623f1c9 and manufactured by COPAN WASP S.R.L.. The authorized representative in Taiwan is PAN ASIA BIOMEDICAL TECHNOLOGY INC..
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