Taiwan FDA registration 5e7d4afdd70b4ded29851a5c93272fae

Pentax Medical endoscopic image processor

TW: “賓得醫療”內視鏡影像處理器
Taiwan flagTaiwan·Risk Class 2·DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.·Registered Oct 10, 2019 – Oct 10, 2029Active
Registration details
Analysis ID
5e7d4afdd70b4ded29851a5c93272fae
Customs Code
DHA05603286301
Company information
Manufacturer Country
Germany;;Japan
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
H Gastroenterology and urology
Product Type (Level 2)
H.1500 Internal Scope and its accessories
Import Information
import
Dates and status
Registration Date
Oct 10, 2019
Expiry Date
Oct 10, 2029
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About this record

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 5e7d4afdd70b4ded29851a5c93272fae and manufactured by DIGITAL ENDOSCOPY GMBH;; HOYA Corporation.. 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., HOYA Corporation.;; PLEXUS MANUFACTURING SDN BHD., 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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