Pure Global

Martin Peter Follicle Stimulating Hormone Diagnostic Kit - Taiwan Registration 97e1ac3aac219973458331c608b6a8dc

Access comprehensive regulatory information for Martin Peter Follicle Stimulating 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 97e1ac3aac219973458331c608b6a8dc 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. 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
97e1ac3aac219973458331c608b6a8dc
Registration Details
Taiwan FDA Registration: 97e1ac3aac219973458331c608b6a8dc
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

Martin Peter Follicle Stimulating Hormone Diagnostic Kit
TW: ้ฆฌไธๅฝผๅพ—ๆฟพๆณกๅˆบๆฟ€ๆฟ€็ด ่จบๆ–ทๅฅ—็ต„
Risk Class 2
Cancelled

Registration Details

97e1ac3aac219973458331c608b6a8dc

DHAS0601653902

Company Information

United States

Product Details

Quantify FSH concentrations in human serum or plasma samples.

A Clinical chemistry and clinical toxicology

A.1300 Follicular Stimulation Hormone Test System

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

May 04, 2006

May 04, 2021

Aug 15, 2023

Cancellation Information

Logged out

่จฑๅฏ่ญ‰ๅทฒ้€พๆœ‰ๆ•ˆๆœŸ