Taiwan FDA registration 52f4916e0ff3c065fd6d620c2bdc3b60
Diasys Lipase Test (Non-Sterile)
TW: 德賽脂肪分解酵素試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Jul 31, 2020 – Jul 31, 2025ExpiredRegistration details
- Analysis ID
- 52f4916e0ff3c065fd6d620c2bdc3b60
- License Form
- Ministry of Health Medical Device Import No. 021808
- Customs Code
- DHA09402180802
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of the Lipolytic Enzyme Test System (A.1465) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1465 Lipolytic enzyme test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 31, 2020
- Expiry Date
- Jul 31, 2025
About this record
Access comprehensive regulatory information for Diasys Lipase Test (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 52f4916e0ff3c065fd6d620c2bdc3b60 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..
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