Taiwan FDA registration f61596939bd37254fef3bae67773de6a
Beckman Coulter Renal Hormone Radioimmunoassay Set
TW: 貝克曼庫爾特腎激素放射免疫分析試劑組
Taiwan·Risk Class 2·IMMUNOTECH S.R.O.·Registered Feb 19, 2016 – Feb 19, 2026ExpiredRegistration details
- Analysis ID
- f61596939bd37254fef3bae67773de6a
- Customs Code
- DHAS5602809205
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
- The content of renal hormone in human plasma was quantified in vitro by 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.1085 Vascular spasmin I
- 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
- Feb 19, 2016
- Expiry Date
- Feb 19, 2026
About this record
Access comprehensive regulatory information for Beckman Coulter Renal Hormone 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 f61596939bd37254fef3bae67773de6a 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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