Taiwan FDA registration e5f8c155ed6eca7cc24146dfd2d8413a
BECKMAN COULTER IGF-I IRMA Kit
TW: 貝克曼庫爾特胰島素生長因子第一型放射免疫分析試劑組
Taiwan·Risk Class 2·MD·IMMUNOTECH S.R.O.·Registered May 26, 2016 – May 26, 2026ExpiredRegistration details
- Analysis ID
- e5f8c155ed6eca7cc24146dfd2d8413a
- License Form
- Ministry of Health Medical Device Import No. 028432
- Customs Code
- DHAS5602843203
Company information
- Manufacturer
- IMMUNOTECH S.R.O.
- Manufacturer Country
- Czechia
- Authorized Representative
- BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.)
Product details
- Intended Use
- In vitro quantification of insulin growth factor type 1 in human serum and plasma using radioimmunoassay.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1370 Human Growth Hormone Test System
- Import Information
- Imported from abroad; Consent must be attached to the input (each input must be supported by the consent of the Atomic Energy Commission)
Dates and status
- Registration Date
- May 26, 2016
- Expiry Date
- May 26, 2026
About this record
Access comprehensive regulatory information for BECKMAN COULTER IGF-I IRMA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e5f8c155ed6eca7cc24146dfd2d8413a and manufactured by IMMUNOTECH S.R.O.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
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