Taiwan FDA registration 5111b2b3ba29280c4d7165fc17f24695

"Pentax" electronic nasopharyngeal endoscope

TW: “賓得士”電子式鼻咽喉內視鏡
Taiwan flagTaiwan·Risk Class 2·HOYA CORPORATION PENTAX MIYAGI FACTORY·Registered Mar 28, 2008 – Mar 28, 2023Expired
Registration details
Analysis ID
5111b2b3ba29280c4d7165fc17f24695
Customs Code
DHA00601876000
Company information
Manufacturer Country
Japan
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order.
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.4760 Nasopharyngeal scopes (soft or rigid) and their accessories
Import Information
import
Dates and status
Registration Date
Mar 28, 2008
Expiry Date
Mar 28, 2023
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About this record

Access comprehensive regulatory information for "Pentax" electronic nasopharyngeal endoscope in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5111b2b3ba29280c4d7165fc17f24695 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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