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Beckman Coulter CellMek SPS Sample Preparation lnstrument (Non-Sterile) - Taiwan Registration 8fc14515d63845f5163f5faf363d0084

Access comprehensive regulatory information for Beckman Coulter CellMek SPS Sample Preparation lnstrument (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 8fc14515d63845f5163f5faf363d0084 and manufactured by Beckman Coulter, Inc.. The authorized representative in Taiwan is BECKMAN COULTER TAIWAN INC., TAIWAN BRANCH (U.S.A.).

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8fc14515d63845f5163f5faf363d0084
Registration Details
Taiwan FDA Registration: 8fc14515d63845f5163f5faf363d0084
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Device Details

Beckman Coulter CellMek SPS Sample Preparation lnstrument (Non-Sterile)
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น CellMek ๆจฃๆœฌ่ฃฝๅ‚™็ณป็ตฑ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

8fc14515d63845f5163f5faf363d0084

Ministry of Health Medical Device Import No. 022944

DHA09402294402

Company Information

United States

Product Details

Limited to the first level identification range of medical equipment classification and grading management method microtitration dilution and dispensing equipment (C.2500).

C Immunology and microbiology

C2500 Microtitration Dilution and Dispensing Equipment

Imported from abroad; GMP

Dates and Status

Nov 07, 2022

Nov 07, 2027