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“Mölnlycke” Mepilex Border Post-Op Ag - Taiwan Registration 77b2a20022a5e47d6c2c7ea1a67853d1

Access comprehensive regulatory information for “Mölnlycke” Mepilex Border Post-Op Ag in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 77b2a20022a5e47d6c2c7ea1a67853d1 and manufactured by Mölnlycke Health Care Oy;;Mölnlycke Health Care AB. The authorized representative in Taiwan is ALSTRONG SCIENTIFIC INTERNATIONAL 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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77b2a20022a5e47d6c2c7ea1a67853d1
Registration Details
Taiwan FDA Registration: 77b2a20022a5e47d6c2c7ea1a67853d1
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Device Details

“Mölnlycke” Mepilex Border Post-Op Ag
TW: “美尼克”美皮蕾防水型術後銀敷料
Risk Class 2
MD

Registration Details

77b2a20022a5e47d6c2c7ea1a67853d1

Ministry of Health Medical Device Import No. 032708

DHA05603270802

Company Information

Product Details

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

I General and plastic surgical devices

I4018 Hydrophilic trauma coverings

Imported from abroad

Dates and Status

Jun 27, 2019

Jun 27, 2024