Taiwan FDA registration 97e1ac3aac219973458331c608b6a8dc

Martin Peter Follicle Stimulating Hormone Diagnostic Kit

TW: 馬丁彼得濾泡刺激激素診斷套組

Taiwan·Risk Class 2·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered May 04, 2006 – May 04, 2021Cancelled

Registration details

Analysis ID: 97e1ac3aac219973458331c608b6a8dc
Customs Code: DHAS0601653902

Company information

Manufacturer: MP BIOMEDICALS DIAGNOSTICS DIVISION
Manufacturer Country: United States
Authorized Representative: GENERAL BIOLOGICALS CORP.

Product details

Intended Use: Quantify FSH concentrations in human serum or plasma samples.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1300 Follicular Stimulation Hormone Test System
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: May 04, 2006
Expiry Date: May 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 Follicle 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 97e1ac3aac219973458331c608b6a8dc and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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