Taiwan FDA registration 5d443ff1970913d5140cb977204ab39e
DiaSys Lactate FS (non-sterile)
TW: 德賽乳酸試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Jul 31, 2020 – Jul 31, 2025ExpiredRegistration details
- Analysis ID
- 5d443ff1970913d5140cb977204ab39e
- License Form
- Ministry of Health Medical Device Import No. 021809
- Customs Code
- DHA09402180901
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 lactate test system (A.1450) of the management measures for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1450 Lactate 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 Lactate FS (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 5d443ff1970913d5140cb977204ab39e and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is MEDITRUST MEDICAL SERVICE & CONSULTANT CO., LTD..
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