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"Aesculap" Manual Surgical Instrument for General Use (Non-Sterile) - Taiwan Registration e2f1f60acbbc35595c7004e28148b528

Access comprehensive regulatory information for "Aesculap" Manual Surgical Instrument for General Use (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 e2f1f60acbbc35595c7004e28148b528 and manufactured by AESCULAP CHIFA SP. Z O.O.. The authorized representative in Taiwan is B. BRAUN TAIWAN CO., LTD..

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e2f1f60acbbc35595c7004e28148b528
Registration Details
Taiwan FDA Registration: e2f1f60acbbc35595c7004e28148b528
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Device Details

"Aesculap" Manual Surgical Instrument for General Use (Non-Sterile)
TW: "้›…ๆฐ"ไธ€่ˆฌๆ‰‹่ก“็”จๆ‰‹ๅ‹•ๅผๅ™จๆขฐ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e2f1f60acbbc35595c7004e28148b528

Ministry of Health Medical Device Import No. 013767

DHA09401376702

Company Information

Poland

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".

I General and plastic surgical devices

I4800 General Surgery Manual Instrument

Imported from abroad

Dates and Status

Jan 09, 2014

Jan 09, 2024