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“Merit” Brighton Bipolar Coagulation Probe - Taiwan Registration bb608d57f2fcadc1247e71567a3033f3

Access comprehensive regulatory information for “Merit” Brighton Bipolar 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 bb608d57f2fcadc1247e71567a3033f3 and manufactured by Merit Medical Systems, Inc.. The authorized representative in Taiwan is Merit Medical Asia Company Limited Taiwan Branch (Hong Kong).

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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Registration Details
Taiwan FDA Registration: bb608d57f2fcadc1247e71567a3033f3
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Device Details

“Merit” Brighton Bipolar Coagulation Probe
TW: “美瑞特”拜博凝血探頭
Risk Class 2
MD

Registration Details

bb608d57f2fcadc1247e71567a3033f3

Ministry of Health Medical Device Import No. 025377

DHA05602537701

Company Information

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

Aug 19, 2013

Aug 19, 2023