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“URGO” SANYRENE spray (Non-Sterile) - Taiwan Registration 54277588c1974736ad4eed033094fa35

Access comprehensive regulatory information for “URGO” SANYRENE spray (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 54277588c1974736ad4eed033094fa35 and manufactured by LABORATOIRES URGO. The authorized representative in Taiwan is ZUELLIG PHARMA, INC..

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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54277588c1974736ad4eed033094fa35
Registration Details
Taiwan FDA Registration: 54277588c1974736ad4eed033094fa35
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Device Details

“URGO” SANYRENE spray (Non-Sterile)
TW: “薾格” 舒立潤壓瘡預防噴劑 (未滅菌)
Risk Class 1
MD

Registration Details

54277588c1974736ad4eed033094fa35

Ministry of Health Medical Device Import No. 014407

DHA09401440703

Company Information

France

Product Details

Limit the first level identification range of liquid bandages (J.5090) of the Measures for the Administration of Medical Devices.

J General hospital and personal use equipment

J5090 Liquid bandages

Imported from abroad; GMP

Dates and Status

Aug 04, 2014

Aug 04, 2024