Taiwan FDA registration 6a6bcdc92f98ecef626fb1711538c0bf

"MORITO" Manual patient transfer device (Non-sterile)

TW: "森戶"手動病患輸送裝置(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·MORITO CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2025Expired
Registration details
Analysis ID
6a6bcdc92f98ecef626fb1711538c0bf
License Form
Ministry of Health Medical Device Import Registration No. 014934
Customs Code
DHA08401493404
Company information
Manufacturer
MORITO CO., LTD.
Manufacturer Country
Japan
Authorized Representative
ZU HUA INTERNATIONAL CO., LTD.
Product details
Intended Use
Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".
Product Type (Level 1)
J General hospital and personal use equipment
Product Type (Level 2)
J6785 Manual Patient Conveyor
Import Information
Imported from abroad
Dates and status
Registration Date
Oct 01, 2021
Expiry Date
Oct 31, 2025
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About this record

Access comprehensive regulatory information for "MORITO" Manual patient transfer device (Non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 6a6bcdc92f98ecef626fb1711538c0bf and manufactured by MORITO CO., LTD.. The authorized representative in Taiwan is ZU HUA INTERNATIONAL CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MORITO CO., LTD., 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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