Taiwan FDA registration 94e643e80b9124f1c344ea8384a527b3
IMMUNOTECH IRMA GH KIT
TW: 伊曼紐特克人體生長激素試劑組
Taiwan·Risk Class 2·MD·IMMUNOTECH S.R.O·Registered Apr 26, 2021 – Apr 26, 2026ExpiredRegistration details
- Analysis ID
- 94e643e80b9124f1c344ea8384a527b3
- License Form
- Ministry of Health Medical Device Import No. 034634
- Customs Code
- DHA05603463406
Company information
- Manufacturer
- IMMUNOTECH S.R.O
- Manufacturer Country
- Czechia
- Authorized Representative
- MEGA BONA INTERNATIONAL CO., LTD.
Product details
- Intended Use
- This product uses extracorporeal radiation immunoassay to determine growth hormone in human serum and plasma.
- 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
- Apr 26, 2021
- Expiry Date
- Apr 26, 2026
About this record
Access comprehensive regulatory information for IMMUNOTECH IRMA GH KIT in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 94e643e80b9124f1c344ea8384a527b3 and manufactured by IMMUNOTECH S.R.O. The authorized representative in Taiwan is MEGA BONA INTERNATIONAL CO., LTD..
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