Taiwan FDA registration 73f1172099deafa82bc951c4080cab5e

"Pentax" electronic colonic endoscope

TW: “賓得士”電子結腸內視鏡
Taiwan flagTaiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Jul 29, 2008 – Jul 29, 2028Active
Registration details
Analysis ID
73f1172099deafa82bc951c4080cab5e
Customs Code
DHA00601913406
Company information
Manufacturer Country
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
Jul 29, 2008
Expiry Date
Jul 29, 2028
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About this record

Access comprehensive regulatory information for "Pentax" electronic colonic endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 73f1172099deafa82bc951c4080cab5e and manufactured by HOYA CORPORATION PENTAX MIYAGI FACTORY. The authorized representative in Taiwan is PENTAX MEDICAL SINGAPORE PTE. LTD. TAIWAN BRANCH(SINGAPORE).

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