Taiwan FDA registration d703f979b65652ef457d2cce72fe5808

Martin Peter Estradiol Hormone Diagnostic Kit

TW: 馬丁彼得雌二醇激素診斷套組
Taiwan flagTaiwan·Risk Class 2·MP BIOMEDICALS LLC DIAGNOSTICS DIVISION·Registered Dec 29, 2005 – Dec 29, 2015Cancelled
Registration details
Analysis ID
d703f979b65652ef457d2cce72fe5808
Customs Code
DHAS0601579502
Company information
Manufacturer Country
United States
Authorized Representative
GENERAL BIOLOGICALS CORP.
Product details
Intended Use
Quantitatively measure the hormone estradiol in human serum or blood.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1260 雌二醇試驗系統
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
Dec 29, 2005
Expiry Date
Dec 29, 2015
Cancellation Date
Apr 21, 2017
Cancellation information
Status
Logged out
Reason
逾期展延
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About this record

Access comprehensive regulatory information for Martin Peter Estradiol 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 d703f979b65652ef457d2cce72fe5808 and manufactured by MP BIOMEDICALS LLC DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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