Taiwan FDA registration 78a74e3a49efb5bce7d633cc1a61d638
Beckman Coulter Human Chorionic Gonadotropin Radioimmunoassay Set
TW: 貝克曼庫爾特人類絨毛膜性腺激素放射免疫分析試劑組
Taiwan·Risk Class 2·IMMUNOTECH S.R.O.·Registered Mar 04, 2016 – Mar 04, 2026ExpiredRegistration details
- Analysis ID
- 78a74e3a49efb5bce7d633cc1a61d638
- Customs Code
- DHAS5602828200
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 total chorionic gonadotropin in human serum and plasma using radioimmunoassay.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1660 Grade Material (Analysis Material Non-Analysis);; A.1150 Calibrated Products;; A.1155 Human chorionic gonadal heterinology
- Import Information
- Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)
Dates and status
- Registration Date
- Mar 04, 2016
- Expiry Date
- Mar 04, 2026
About this record
Access comprehensive regulatory information for Beckman Coulter Human Chorionic Gonadotropin Radioimmunoassay Set in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 78a74e3a49efb5bce7d633cc1a61d638 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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