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“FINEMEDIX” Single-Use Clear-Hemostat Coagulation Probe - Taiwan Registration 46002cbd2a3461743a44dd25afe21a27

Access comprehensive regulatory information for “FINEMEDIX” Single-Use Clear-Hemostat Coagulation Probe in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 46002cbd2a3461743a44dd25afe21a27 and manufactured by FINEMEDIX CO., LTD. The authorized representative in Taiwan is SCHMIDT SCIENTIFIC TAIWAN LTD..

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46002cbd2a3461743a44dd25afe21a27
Registration Details
Taiwan FDA Registration: 46002cbd2a3461743a44dd25afe21a27
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Device Details

“FINEMEDIX” Single-Use Clear-Hemostat Coagulation Probe
TW: “汎美德斯”單次用凝血探頭
Risk Class 2
MD

Registration Details

46002cbd2a3461743a44dd25afe21a27

Ministry of Health Medical Device Import No. 033622

DHA05603362207

Company Information

Korea, Republic of

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology-urology devices

H4300 Electrocutors for endoscopes and accessories

Imported from abroad

Dates and Status

May 05, 2020

May 05, 2025