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SANKEN AITERNATING PRESSURE AIR FLOTATION MATTRESS (NON-STERILE) - Taiwan Registration 1d5364ebf1ab9b6562f558c9c1e90f0c

Access comprehensive regulatory information for SANKEN AITERNATING PRESSURE AIR FLOTATION MATTRESS (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 1d5364ebf1ab9b6562f558c9c1e90f0c and manufactured by SANWA KAKEN KOGYO CO., LTD.. The authorized representative in Taiwan is HURN ARNG ENTERPRISE CO., LTD..

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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1d5364ebf1ab9b6562f558c9c1e90f0c
Registration Details
Taiwan FDA Registration: 1d5364ebf1ab9b6562f558c9c1e90f0c
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Device Details

SANKEN AITERNATING PRESSURE AIR FLOTATION MATTRESS (NON-STERILE)
TW: ไธ‰็ ”ไบคๆ›ฟๅผๅฃ“ๅŠ›ๆฐฃๅขŠๅบŠ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

1d5364ebf1ab9b6562f558c9c1e90f0c

Ministry of Health Medical Device Import No. 015349

DHA09401534907

Company Information

Product Details

J General hospital and personal use equipment

J5550 Alternating pressure air mattress

Imported from abroad

Dates and Status

Jun 16, 2015

Jun 16, 2020

Jun 22, 2022

Cancellation Information

Logged out

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