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Martin Peter Estradiol Hormone Diagnostic Kit - Taiwan Registration d703f979b65652ef457d2cce72fe5808

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..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MP BIOMEDICALS 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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d703f979b65652ef457d2cce72fe5808
Registration Details
Taiwan FDA Registration: d703f979b65652ef457d2cce72fe5808
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Device Details

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

Registration Details

d703f979b65652ef457d2cce72fe5808

DHAS0601579502

Company Information

Product Details

Quantitatively measure the hormone estradiol in human serum or blood.

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

Dec 29, 2005

Dec 29, 2015

Apr 21, 2017

Cancellation Information

Logged out

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