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“PAJUNK” SonoPlex Stim Cannula - Taiwan Registration ab6953e91bcac9b356d7921ad9d21062

Access comprehensive regulatory information for “PAJUNK” SonoPlex Stim Cannula in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab6953e91bcac9b356d7921ad9d21062 and manufactured by PAJUNK GMBH MEDIZINTECHNOLOGIE. The authorized representative in Taiwan is Huizhong Co., Ltd.

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ab6953e91bcac9b356d7921ad9d21062
Registration Details
Taiwan FDA Registration: ab6953e91bcac9b356d7921ad9d21062
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Device Details

“PAJUNK” SonoPlex Stim Cannula
TW: “帕將克”超音波導引神經阻斷導管組
Risk Class 2
MD

Registration Details

ab6953e91bcac9b356d7921ad9d21062

Ministry of Health Medical Device Import No. 025441

DHA05602544107

Company Information

Product Details

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

D Devices for anesthesiology

D5140 Anesthesia Transport Group

Imported from abroad

Dates and Status

Oct 23, 2013

Oct 23, 2028