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“PENTAX” VIDEO DUODENOSCOPE - Taiwan Registration bfeb730fed9c8abc59c9321132b87476

Access comprehensive regulatory information for “PENTAX” VIDEO DUODENOSCOPE in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number bfeb730fed9c8abc59c9321132b87476 and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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bfeb730fed9c8abc59c9321132b87476
Registration Details
Taiwan FDA Registration: bfeb730fed9c8abc59c9321132b87476
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Device Details

“PENTAX” VIDEO DUODENOSCOPE
TW: “賓得”電子十二指腸內視鏡
Risk Class 2
MD

Registration Details

bfeb730fed9c8abc59c9321132b87476

Ministry of Health Medical Device Import No. 027130

DHA05602713000

Product Details

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

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Mar 10, 2015

Mar 10, 2025