“SEAWON” Veeler Video Guided Catheter
Taiwan·Risk Class 2·MD·SEAWON MEDITECH CO., LTD.·Registered Aug 10, 2015 – Aug 10, 2020Cancelled- Analysis ID
- 4ffe7ea5e23934ff39641353f0ab0bcb
- License Form
- Ministry of Health Medical Device Import No. 027587
- Customs Code
- DHA05602758706
- Manufacturer
- SEAWON MEDITECH CO., LTD.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- KROMAX INTERNATIONAL CORP.
- Product Type (Level 1)
- D Devices for anesthesiology
- Product Type (Level 2)
- D5120 Anesthesia delivery catheter
- Import Information
- Imported from abroad
- Registration Date
- Aug 10, 2015
- Expiry Date
- Aug 10, 2020
- Cancellation Date
- Jul 15, 2022
- Status
- Logged out
- Reason
- 未展延而逾期者
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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 4ffe7ea5e23934ff39641353f0ab0bcb and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is KROMAX INTERNATIONAL CORP..
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.