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Sanquin Preservation medium (non-sterile) - Taiwan Registration 7f25a303c078e41a8e01c08838aca033

Access comprehensive regulatory information for Sanquin Preservation 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 7f25a303c078e41a8e01c08838aca033 and manufactured by SANQUIN REAGENTS B.V.. The authorized representative in Taiwan is METEK LAB 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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7f25a303c078e41a8e01c08838aca033
Registration Details
Taiwan FDA Registration: 7f25a303c078e41a8e01c08838aca033
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Device Details

Sanquin Preservation medium (non-sterile)
TW: ๆฃฎๅฅŽๆฉ ็ด…่ก€็ƒไฟๅญ˜ๆถฒ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

7f25a303c078e41a8e01c08838aca033

Ministry of Health Medical Device Import No. 017862

DHA09401786203

Company Information

Netherlands

Product Details

Limited to the first level identification range of blood cell thinners (B.8200) of the management methods for medical devices.

B Hematology and pathology devices

B8200 Blood cell thinner

Imported from abroad

Dates and Status

May 19, 2017

May 19, 2022