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Pentax Medical endoscopic image processor - Taiwan Registration 12e8e1f6395d54252ede803f3c159f1c

Access comprehensive regulatory information for Pentax Medical endoscopic image processor in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 12e8e1f6395d54252ede803f3c159f1c and manufactured by HOYA Corporation.;; PLEXUS MANUFACTURING SDN BHD.. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

This page provides complete technical specifications, regulatory compliance details, 2 companies making similar products including Plexus Manufacturing Sdn. Bhd.;; HOYA Corporation., DIGITAL ENDOSCOPY GMBH;; HOYA Corporation., and 4 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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12e8e1f6395d54252ede803f3c159f1c
Registration Details
Taiwan FDA Registration: 12e8e1f6395d54252ede803f3c159f1c
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Device Details

Pentax Medical endoscopic image processor
TW: โ€œ่ณ“ๅพ—้†ซ็™‚โ€ๅ…ง่ฆ–้กๅฝฑๅƒ่™•็†ๅ™จ
Risk Class 2

Registration Details

12e8e1f6395d54252ede803f3c159f1c

DHA05603302301

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

Contract manufacturing;; input

Dates and Status

Dec 16, 2019

Dec 16, 2024

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