Taiwan FDA registration 5a73025b47afb29256821ff9ee514d6a
Martin Peter Cortisol Diagnostic Kit
TW: 馬丁彼得皮質醇診斷套組
Taiwan·Risk Class 2·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Mar 29, 2006 – Mar 29, 2021CancelledRegistration details
- Analysis ID
- 5a73025b47afb29256821ff9ee514d6a
- Customs Code
- DHAS0601624801
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Used to measure cortisol concentrations in unextracted serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1205 Cortisol (hydronephrine, and hydroxycortisol) test system
- 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 29, 2006
- Expiry Date
- Mar 29, 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 Cortisol 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 5a73025b47afb29256821ff9ee514d6a and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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