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“Seawon” Veeler Video Guided Catheter - Taiwan Registration 5cfea577673dc3672dab04be0ba0edff

Access comprehensive regulatory information for “Seawon” Veeler Video Guided Catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 5cfea577673dc3672dab04be0ba0edff and manufactured by Seawon Meditech Co., Ltd.. The authorized representative in Taiwan is BUTICON INTERNATIONAL CORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including SEAWON MEDITECH CO., LTD., and 1 recent registrations in the same category. 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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5cfea577673dc3672dab04be0ba0edff
Registration Details
Taiwan FDA Registration: 5cfea577673dc3672dab04be0ba0edff
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Device Details

“Seawon” Veeler Video Guided Catheter
TW: “希旺”費拉影像硬脊膜導管
Risk Class 2
MD

Registration Details

5cfea577673dc3672dab04be0ba0edff

Ministry of Health Medical Device Import No. 030793

DHA05603079306

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

Apr 02, 2018

Apr 02, 2028

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