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GB hCG EIA Kit - Taiwan Registration 79d2261984e81f04c8843676c6f5d026

Access comprehensive regulatory information for GB hCG EIA Kit in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 79d2261984e81f04c8843676c6f5d026 and manufactured by BioCheck, Inc.. 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.

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79d2261984e81f04c8843676c6f5d026
Registration Details
Taiwan FDA Registration: 79d2261984e81f04c8843676c6f5d026
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Device Details

GB hCG EIA Kit
TW: ๆ™ฎ็”Ÿไบบ้กž็ตจๆฏ›่†œไฟƒๆ€ง่…บๆฟ€็ด ้…ต็ด ๅ…็–ซๅˆ†ๆžๅฅ—็ต„
Risk Class 2
MD
Cancelled

Registration Details

79d2261984e81f04c8843676c6f5d026

Ministry of Health Medical Device Import No. 026535

DHA05602653508

Company Information

United States

Product Details

A Clinical chemistry and clinical toxicology

A1155 Human chorionic gonadotropin test system

Imported from abroad

Dates and Status

Sep 22, 2014

Sep 22, 2024

May 17, 2023

Cancellation Information

Logged out

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