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LEIBO Synthetic Cell & Tissue Culture Media & Ingredients (Sterilized) - Taiwan Registration c789853d8601a67c129c84025bbf0c70

Access comprehensive regulatory information for LEIBO Synthetic Cell & Tissue Culture Media & Ingredients (Sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number c789853d8601a67c129c84025bbf0c70 and manufactured by FUJIFILM Irvine Scientific, Inc.. The authorized representative in Taiwan is LabIVF Taiwan International Co., Ltd.

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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c789853d8601a67c129c84025bbf0c70
Registration Details
Taiwan FDA Registration: c789853d8601a67c129c84025bbf0c70
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Device Details

LEIBO Synthetic Cell & Tissue Culture Media & Ingredients (Sterilized)
TW: ใ€็ฃŠๆŸใ€žๅˆๆˆ็ดฐ่ƒžๅ’Œ็ต„็น”ๅŸน้คŠๅŸบๅŠๆˆไปฝ (ๆป…่Œ)
Risk Class 1

Registration Details

c789853d8601a67c129c84025bbf0c70

DHA09402339000

Company Information

United States

Product Details

It is limited to the first level of identification of synthetic cell and tissue culture media and ingredients (B.2220) in the classification and grading management measures for medical devices.

B Hematology, pathology, and genetics

B.2220 Synthetic cell and tissue culture media and components

QMS/QSD;; ่ผธๅ…ฅ

Dates and Status

Feb 19, 2024

Feb 19, 2029