Taiwan FDA registration dede207c64b22e6451546b3171a88fc8
Greenfield Automatic Enzyme Immunoassay (Unsterilized)
TW: 葛林弗全自動酵素免疫分析儀(未滅菌)
Taiwan·Risk Class 1·DIAGNOSTIC GRIFOLS S.A.·Registered Oct 25, 2006 – Oct 25, 2021CancelledRegistration details
- Analysis ID
- dede207c64b22e6451546b3171a88fc8
- Customs Code
- DHA04400526400
Company information
- Manufacturer
- DIAGNOSTIC GRIFOLS S.A.
- Manufacturer Country
- Spain
- Authorized Representative
- EVERLIGHT BIOTECH(TAIWAN) CO., LTD.
Product details
- Intended Use
- Limited to the first level identification range of enzyme analyzer for clinical use (A.2500) of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2500 Enzyme analyzer for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Oct 25, 2006
- Expiry Date
- Oct 25, 2021
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Greenfield Automatic Enzyme Immunoassay (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number dede207c64b22e6451546b3171a88fc8 and manufactured by DIAGNOSTIC GRIFOLS S.A.. The authorized representative in Taiwan is EVERLIGHT BIOTECH(TAIWAN) CO., LTD..
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