Taiwan FDA registration e29ec93d9e47430274b78c26224a72fc
Pushen Gastrine Hormone Radioimmunoassay Reagent (Unsterilized)
TW: 普生 胃泌激素放射免疫分析試劑(未滅菌)
Taiwan·Risk Class 1·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Sep 05, 2005 – Sep 05, 2025ExpiredRegistration details
- Analysis ID
- e29ec93d9e47430274b78c26224a72fc
- Customs Code
- DHAS4400037801
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- It is used to measure the immunoreactive gastrin content in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1325 胃泌素試驗系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Sep 05, 2005
- Expiry Date
- Sep 05, 2025
About this record
Access comprehensive regulatory information for Pushen Gastrine Hormone Radioimmunoassay Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e29ec93d9e47430274b78c26224a72fc and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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