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"Acerys" double-tube syringe system - Taiwan Registration 28050d2f7cad13b647247d67f7c248b4

Access comprehensive regulatory information for "Acerys" double-tube syringe system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 28050d2f7cad13b647247d67f7c248b4 and manufactured by TRANSCOJECT GMBH;; Arthrex, Inc.. The authorized representative in Taiwan is JOINSMART BIOMEDICAL COMPANY LIMITED.

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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28050d2f7cad13b647247d67f7c248b4
Registration Details
Taiwan FDA Registration: 28050d2f7cad13b647247d67f7c248b4
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Device Details

"Acerys" double-tube syringe system
TW: โ€œ่‰พๆ€็‘žๆ–ฏโ€้›™็ฎกๆณจๅฐ„ๅ™จ็ณป็ตฑ
Risk Class 2

Registration Details

28050d2f7cad13b647247d67f7c248b4

DHA05602690604

Company Information

United States;;Germany

Product Details

For details, it is Chinese approved copy of the imitation order

J General hospital and personal use equipment

J.5860 ๆดปๅกžๅผๆณจๅฐ„็ญ’

import

Dates and Status

Jan 08, 2015

Jan 08, 2030