“Seawon” Veeler Video Guided Catheter
Taiwan·Risk Class 2·MD·Seawon Meditech Co., Ltd.·Registered Apr 02, 2018 – Apr 02, 2028Active- Analysis ID
- 5cfea577673dc3672dab04be0ba0edff
- License Form
- Ministry of Health Medical Device Import No. 030793
- Customs Code
- DHA05603079306
- Manufacturer
- Seawon Meditech Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- BUTICON INTERNATIONAL CORPORATION
- Intended Use
- For details, it is Chinese approved copy of the imitation order
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5120 Anesthesia delivery catheter
- Import Information
- Imported from abroad
- Registration Date
- Apr 02, 2018
- Expiry Date
- Apr 02, 2028
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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.