“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.
Device Details
Registration Details
5cfea577673dc3672dab04be0ba0edff
Ministry of Health Medical Device Import No. 030793
DHA05603079306
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

