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“SEAWON” St. Reed Steerable Neurolysis Catheter System - Taiwan Registration 08131be5de99b15a9f3d47c2d1f39798

Access comprehensive regulatory information for “SEAWON” St. Reed Steerable Neurolysis Catheter System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 08131be5de99b15a9f3d47c2d1f39798 and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is JUBILANT SUNRISE SCIENTIFIC CO., LTD..

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08131be5de99b15a9f3d47c2d1f39798
Registration Details
Taiwan FDA Registration: 08131be5de99b15a9f3d47c2d1f39798
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Device Details

“SEAWON” St. Reed Steerable Neurolysis Catheter System
TW: “喜旺”史瑞德活動式硬膜外導管
Risk Class 2
MD

Registration Details

08131be5de99b15a9f3d47c2d1f39798

Ministry of Health Medical Device Import No. 025215

DHA05602521501

Company Information

Korea, Republic of

Product Details

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

D Devices for anesthesiology

D5120 Anesthesia delivery catheter

Imported from abroad

Dates and Status

Jul 29, 2013

Jul 29, 2023