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"Jianpeng" manual patient transport device (unsterilized) - Taiwan Registration 608ecafd88b7374ec0630722fbf53b1f

Access comprehensive regulatory information for "Jianpeng" 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 608ecafd88b7374ec0630722fbf53b1f and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is J. P. CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Xincheng Seat Cushion Co., Ltd.;; Jianpeng Trading 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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608ecafd88b7374ec0630722fbf53b1f
Registration Details
Taiwan FDA Registration: 608ecafd88b7374ec0630722fbf53b1f
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Device Details

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

Registration Details

608ecafd88b7374ec0630722fbf53b1f

Company Information

Taiwan, Province of China

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

Domestic;; Contract manufacturing

Dates and Status

Oct 08, 2019

Oct 08, 2024

Sep 30, 2021

Cancellation Information

Logged out

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