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"Seawon" Lymphocyte separation medium (NON-Sterile) - Taiwan Registration c9f89a0973bfa493c26a9fa2138ea114

Access comprehensive regulatory information for "Seawon" Lymphocyte separation medium (NON-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c9f89a0973bfa493c26a9fa2138ea114 and manufactured by SEAWON MEDITECH CO., LTD.. The authorized representative in Taiwan is GREAT RIVER LIFECARE INC..

This page provides complete technical specifications, regulatory compliance details. 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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c9f89a0973bfa493c26a9fa2138ea114
Registration Details
Taiwan FDA Registration: c9f89a0973bfa493c26a9fa2138ea114
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Device Details

"Seawon" Lymphocyte separation medium (NON-Sterile)
TW: "่†ๆœ›" ๆท‹ๅทด็ƒๅˆ†้›ขๅŸน้คŠๅŸบ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

c9f89a0973bfa493c26a9fa2138ea114

Ministry of Health Medical Device Import No. 016661

DHA09401666101

Company Information

Korea, Republic of

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Devices "Lymphocyte Separation Medium (B.8500)".

B Hematology and pathology devices

B8500 Lymphocyte Isolation Medium

Imported from abroad

Dates and Status

Jun 17, 2016

Jun 17, 2021