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LUMIPULSE G1200 (Non-Sterile) - Taiwan Registration 2c2cb8996b9a5a5c711949be0c85d669

Access comprehensive regulatory information for LUMIPULSE G1200 (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2c2cb8996b9a5a5c711949be0c85d669 and manufactured by OTSUKA ELECTRONICS CO., LTD. SHIGA FACTORY. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.

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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2c2cb8996b9a5a5c711949be0c85d669
Registration Details
Taiwan FDA Registration: 2c2cb8996b9a5a5c711949be0c85d669
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Device Details

LUMIPULSE G1200 (Non-Sterile)
TW: ้Œ„็ง˜ๅธ•ๆ–ฏG1200 ๅŒ–ๅญธๅ†ทๅ…‰ๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

2c2cb8996b9a5a5c711949be0c85d669

Ministry of Health Medical Device Import Registration No. 009828

DHA08400982801

Company Information

Product Details

A Clinical chemistry and clinical toxicology

A2160 Individual photometric chemistry analyzer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2026

Oct 28, 2022

Cancellation Information

Logged out

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