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KOHKEN Rescue Stretcher (Non-sterile) - Taiwan Registration 645022f67ec29dc32e6e814237fe7d8c

Access comprehensive regulatory information for KOHKEN Rescue Stretcher (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 645022f67ec29dc32e6e814237fe7d8c and manufactured by KOHKEN Inc.. The authorized representative in Taiwan is SALVO ENTERPRISE CORP..

This page provides complete technical specifications, regulatory compliance details. 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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645022f67ec29dc32e6e814237fe7d8c
Registration Details
Taiwan FDA Registration: 645022f67ec29dc32e6e814237fe7d8c
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Device Details

KOHKEN Rescue Stretcher (Non-sterile)
TW: ๅ…‰็ ” ไพฟๆ”œๅผๆ“”ๆžถ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

645022f67ec29dc32e6e814237fe7d8c

Ministry of Health Medical Device Import Registration No. a00104

DHA084a0010409

Company Information

Japan

Product Details

Limited to the first level identification scope of the "portable stretcher (J.6900)" of the Measures for the Classification and Grading Management of Medical Equipment.

J General hospital and personal use equipment

J6900 portable stretcher

Dates and Status

Sep 01, 2022

Oct 31, 2023