Taiwan FDA registration a161068ba5a499007760322b7acf19c2
"Diasys" ALAT (GPT) FS (Non-Sterile)
TW: "德信" 胺基丙酸轉移酶檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Feb 01, 2018 – Feb 01, 2028ActiveRegistration details
- Analysis ID
- a161068ba5a499007760322b7acf19c2
- License Form
- Ministry of Health Medical Device Import No. 018788
- Customs Code
- DHA09401878809
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of the propylaminotransferase test system (A.1030) of the management method for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1030 Alpine transaminase test system
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Feb 01, 2018
- Expiry Date
- Feb 01, 2028
About this record
Access comprehensive regulatory information for "Diasys" ALAT (GPT) 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 a161068ba5a499007760322b7acf19c2 and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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