Taiwan FDA registration 274d9483750d8e79571e18425541eb9c
“Diasys” ASAT (GOT) FS
TW: “德信” 天門冬胺酸轉移酶檢驗試劑
Taiwan·Risk Class 2·MD·DIASYS DIAGNOSTIC SYSTEMS GMBH·Registered Dec 26, 2017 – Dec 26, 2027ActiveRegistration details
- Analysis ID
- 274d9483750d8e79571e18425541eb9c
- License Form
- Ministry of Health Medical Device Import No. 030472
- Customs Code
- DHA05603047202
Company information
- Manufacturer
- DIASYS DIAGNOSTIC SYSTEMS GMBH
- Manufacturer Country
- Germany
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- This product is used with an optical colorimetric analyzer to quantitatively detect the concentration of aspartine transferase in serum or plasma in vitro.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1100 Aspartine Transfer Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Dec 26, 2017
- Expiry Date
- Dec 26, 2027
About this record
Access comprehensive regulatory information for “Diasys” ASAT (GOT) FS in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 274d9483750d8e79571e18425541eb9c and manufactured by DIASYS DIAGNOSTIC SYSTEMS GMBH. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices