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“Mölnlycke” Granulox Woundspray - Taiwan Registration dc5b23077a23e3d422fee33563a56aea

Access comprehensive regulatory information for “Mölnlycke” Granulox Woundspray in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number dc5b23077a23e3d422fee33563a56aea and manufactured by Hälsa Pharma GmbH. The authorized representative in Taiwan is MOLNLYCKE HEALTH CARE TAIWAN CO., LTD..

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dc5b23077a23e3d422fee33563a56aea
Registration Details
Taiwan FDA Registration: dc5b23077a23e3d422fee33563a56aea
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Device Details

“Mölnlycke” Granulox Woundspray
TW: “墨尼克”氧療舒傷口噴劑
Risk Class 3
MD

Registration Details

dc5b23077a23e3d422fee33563a56aea

Ministry of Health Medical Device Import No. 030980

DHA05603098005

Company Information

Germany

Product Details

This product is suitable for the treatment of chronic wounds, such as venous ulcers on the legs, arterial ulcers, mixed ulcers, diabetic foot ulcers, secondary healing surgical wounds, and pressure injuries (pressure ulcers), and can also be used for wounds of debridement of carrion and infectious tissues.

I General and plastic surgical devices

Imported from abroad

Dates and Status

Jun 13, 2018

Jun 13, 2028