Taiwan FDA registration decdc33574366cf7d2759f0024a56f9a

"Pentax" electronic duodenal endoscope

TW: "賓得士"電子十二指腸內視鏡
Taiwan flagTaiwan·PENTAX TOHOKU CO., LTD.·Registered Mar 29, 2006 – Mar 29, 2011Cancelled
Registration details
Analysis ID
decdc33574366cf7d2759f0024a56f9a
Customs Code
DHA00601421507
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
Import Information
import
Dates and status
Registration Date
Mar 29, 2006
Expiry Date
Mar 29, 2011
Cancellation Date
Jul 25, 2014
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" electronic duodenal endoscope in Taiwan's medical device market through Pure Global AI's free database. is registered under number decdc33574366cf7d2759f0024a56f9a and manufactured by PENTAX TOHOKU CO., LTD.. 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 MIYAGI 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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