Taiwan FDA registration 6a6c74905cf8d0f02bfff83225331af3

Martin Peter Lactation Hormone Diagnostic Kit

TW: 馬丁彼得泌乳激素診斷套組

Taiwan·Risk Class 2·MP BIOMEDICALS LLC DIAGNOSTICS DIVISION·Registered Dec 29, 2005 – Dec 29, 2015Cancelled

Registration details

Analysis ID: 6a6c74905cf8d0f02bfff83225331af3
Customs Code: DHAS0601579400

Company information

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

Product details

Intended Use: The prolactin test suite is a radioimmunoassay designed for the extracorporeal quantification of human serum prolactin.
Product Type (Level 1): A Clinical chemistry and clinical toxicology
Product Type (Level 2): A.1625 Prolactin 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: Dec 29, 2005
Expiry Date: Dec 29, 2015
Cancellation Date: Jun 28, 2018

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for Martin Peter Lactation 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 6a6c74905cf8d0f02bfff83225331af3 and manufactured by MP BIOMEDICALS LLC DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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