Taiwan FDA registration 1ddb73ba4afa61ea7fc877f07c1cb486

Image processor for Pentax endoscopes

TW: “賓得士”內視鏡用影像處理器
Taiwan flagTaiwan·Risk Class 2·HOYA CORPORATION PENTAX YAMAGATA FACTORY·Registered Oct 21, 2010 – Oct 21, 2015Cancelled
Registration details
Analysis ID
1ddb73ba4afa61ea7fc877f07c1cb486
Customs Code
DHA00602158709
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
Oct 21, 2010
Expiry Date
Oct 21, 2015
Cancellation Date
May 28, 2018
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 Image processor for Pentax endoscopes in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1ddb73ba4afa61ea7fc877f07c1cb486 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, 2 companies making similar products including PENTAX TOHOKU CO., LTD. YAMAGATA FACTORY, HOYA CORPORATION PENTAX YAMAGATA FACTORY, and 2 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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