Taiwan FDA registration a22947075ebb915b68caedb8b8b86cd5

"Pentax" endoscopic image processor

TW: “賓得士”內視鏡影像處理器
Taiwan flagTaiwan·Risk Class 2·HOYA CORPORATION PENTAX YAMAGATA FACTORY·Registered May 22, 2008 – May 22, 2018Cancelled
Registration details
Analysis ID
a22947075ebb915b68caedb8b8b86cd5
Customs Code
DHA00601886300
Company information
Manufacturer Country
Japan
Authorized Representative
WHOLE WELL CO., LTD.
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
May 22, 2008
Expiry Date
May 22, 2018
Cancellation Date
Dec 13, 2019
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for "Pentax" 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 a22947075ebb915b68caedb8b8b86cd5 and manufactured by HOYA CORPORATION PENTAX YAMAGATA FACTORY. The authorized representative in Taiwan is WHOLE WELL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HOYA CORPORATION PENTAX YAMAGATA FACTORY, and 1 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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