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“AFS” Sterile Single-use Access Port for Surgery - Taiwan Registration 0a4f0d702f3620f2872d4a74ac9d8f9c

Access comprehensive regulatory information for “AFS” Sterile Single-use Access Port for Surgery in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0a4f0d702f3620f2872d4a74ac9d8f9c and manufactured by AFS Medical Co., Ltd.. The authorized representative in Taiwan is Huizhong 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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0a4f0d702f3620f2872d4a74ac9d8f9c
Registration Details
Taiwan FDA Registration: 0a4f0d702f3620f2872d4a74ac9d8f9c
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Device Details

“AFS” Sterile Single-use Access Port for Surgery
TW: “艾弗思”單次使用多器械導入套管組
Risk Class 2
MD

Registration Details

0a4f0d702f3620f2872d4a74ac9d8f9c

Ministry of Health Medical Device Import No. 034987

DHA05603498700

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

H Gastroenterology-urology devices

H1500 endoscope and accessories

Imported from abroad

Dates and Status

Oct 25, 2021

Oct 25, 2026