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“PENTAX”SNARE - Taiwan Registration 139bb374ec422617d87a3a01c8140d96

Access comprehensive regulatory information for “PENTAX”SNARE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 139bb374ec422617d87a3a01c8140d96 and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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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139bb374ec422617d87a3a01c8140d96
Registration Details
Taiwan FDA Registration: 139bb374ec422617d87a3a01c8140d96
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Device Details

“PENTAX”SNARE
TW: “賓得”切除環
Risk Class 2
MD

Registration Details

139bb374ec422617d87a3a01c8140d96

Ministry of Health Medical Device Import No. 029224

DHA05602922406

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

Dec 22, 2016

Dec 22, 2021