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"FUJI" DRI-CHEM IMMUNO AG1 (Non-Sterile) - Taiwan Registration 2846d3b725bb90ea715adb2666ce3417

Access comprehensive regulatory information for "FUJI" DRI-CHEM IMMUNO AG1 (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 2846d3b725bb90ea715adb2666ce3417 and manufactured by TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY. The authorized representative in Taiwan is HUNG CHONG CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TERASAKI ELECTRIC CO., LTD. SYSTEM DIV. YAO FACTORY, 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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2846d3b725bb90ea715adb2666ce3417
Registration Details
Taiwan FDA Registration: 2846d3b725bb90ea715adb2666ce3417
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Device Details

"FUJI" DRI-CHEM IMMUNO AG1 (Non-Sterile)
TW: "ๅฏŒๅฃซ"ไนพๅผๅ…็–ซๅˆ†ๆžๅ„€(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

2846d3b725bb90ea715adb2666ce3417

Ministry of Health Medical Device Import Registration No. 018792

DHA08401879204

Company Information

Product Details

Limited to the first level identification range of "Colorimeter, Photometer or Spectrophotometer for Clinical Use (A.2300)" under the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A2300 Colorimeter, photometer, or spectrophotometer for clinical use

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023

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