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"Regemini" manual patient transport device (unsterilized) - Taiwan Registration e794899bdb47d8c2f262e009483e81b3

Access comprehensive regulatory information for "Regemini" manual patient transport device (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e794899bdb47d8c2f262e009483e81b3 and manufactured by CHANGZHOU LAIJIE HEALTH MATERIALS CO., LTD.. The authorized representative in Taiwan is FUROTO MEDICAL & WELFARE CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including CHANGZHOU LAIJIE HEALTH MATERIALS 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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e794899bdb47d8c2f262e009483e81b3
Registration Details
Taiwan FDA Registration: e794899bdb47d8c2f262e009483e81b3
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Device Details

"Regemini" manual patient transport device (unsterilized)
TW: "่Šๆท" ๆ‰‹ๅ‹•็—…ๆ‚ฃ่ผธ้€่ฃ็ฝฎ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e794899bdb47d8c2f262e009483e81b3

DHA09600373308

Company Information

Product Details

Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Manual Patient Transport Device (J.6785)".

J General hospital and personal use equipment

J.6785 Manual Patient Conveying Device

Input;; Chinese goods

Dates and Status

Mar 21, 2019

Mar 21, 2024

Sep 30, 2021

Cancellation Information

Logged out

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