Taiwan FDA registration a33be6c2d00a2db2a6654dc489c92cd4
Martin Peter Thyroid Stimulating Hormone Diagnostic Kit
TW: 馬丁彼得甲狀腺刺激激素診斷套組
Taiwan·Risk Class 2·MP Biomedicals Diagnostics Division·Registered Apr 04, 2006 – Apr 04, 2021CancelledRegistration details
- Analysis ID
- a33be6c2d00a2db2a6654dc489c92cd4
- Customs Code
- DHAS0601628902
Company information
- Manufacturer
- MP Biomedicals Diagnostics Division
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Radioimmunoassay designed to quantify TSH concentrations in human serum or plasma samples.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1695 游離甲狀腺素試驗系統
- Import Information
- Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
- Registration Date
- Apr 04, 2006
- Expiry Date
- Apr 04, 2021
- Cancellation Date
- Aug 15, 2023
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Martin Peter Thyroid Stimulating Hormone Diagnostic Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a33be6c2d00a2db2a6654dc489c92cd4 and manufactured by MP Biomedicals Diagnostics Division. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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