Taiwan FDA registration 1970f04364215c95ad42ec4994094b4a

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 DIAGNOSTICS DIVISION·Registered Apr 14, 2017 – Apr 14, 2027Active
Registration details
Analysis ID
1970f04364215c95ad42ec4994094b4a
Customs Code
DHAS5602954304
Company information
Manufacturer Country
United States
Authorized Representative
GENERAL BIOLOGICALS CORP.
Product details
Intended Use
Quantitative detection of estradiol hormone in human serum or plasma.
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
Apr 14, 2017
Expiry Date
Apr 14, 2027
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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 1970f04364215c95ad42ec4994094b4a and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MP BIOMEDICALS LLC DIAGNOSTICS DIVISION, and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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