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Martin Peter Estradiol Hormone Diagnostic Kit - Taiwan Registration 1970f04364215c95ad42ec4994094b4a

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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1970f04364215c95ad42ec4994094b4a
Registration Details
Taiwan FDA Registration: 1970f04364215c95ad42ec4994094b4a
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Device Details

Martin Peter Estradiol Hormone Diagnostic Kit
TW: ้ฆฌไธๅฝผๅพ—้›ŒไบŒ้†‡ๆฟ€็ด ่จบๆ–ทๅฅ—็ต„
Risk Class 2

Registration Details

1970f04364215c95ad42ec4994094b4a

DHAS5602954304

Company Information

United States

Product Details

Quantitative detection of estradiol hormone in human serum or plasma.

A Clinical chemistry and clinical toxicology

A.1260 ้›ŒไบŒ้†‡่ฉฆ้ฉ—็ณป็ตฑ

Input;; Consent letter must be attached to the import (consent from the Atomic Energy Commission must be obtained for each import)

Dates and Status

Apr 14, 2017

Apr 14, 2027

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