Taiwan FDA registration 135d94700cb13253db68105caaa8f228
Beckman Coulter angioconstrictin I radioimmunoassay reagent
TW: 貝克曼庫爾特血管收縮素I放射免疫分析試劑
Taiwan·Risk Class 2·IMMUNOTECH S.R.O.·Registered Feb 03, 2017 – Feb 03, 2027ActiveRegistration details
- Analysis ID
- 135d94700cb13253db68105caaa8f228
- Customs Code
- DHAS5602931800
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
- Quantitative analysis of renin activity in human 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.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 03, 2017
- Expiry Date
- Feb 03, 2027
About this record
Access comprehensive regulatory information for Beckman Coulter angioconstrictin I radioimmunoassay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 135d94700cb13253db68105caaa8f228 and manufactured by IMMUNOTECH S.R.O.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).
This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.
Free DatabasePowered by Pure Global AI89,000+ Devices