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Beckman Coulter AQUIOS Tetra-1 & Tetra-2+ Panel - Taiwan Registration a1473df243fa2ea4a364538ff6543d46

Access comprehensive regulatory information for Beckman Coulter AQUIOS Tetra-1 & Tetra-2+ Panel in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number a1473df243fa2ea4a364538ff6543d46 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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a1473df243fa2ea4a364538ff6543d46
Registration Details
Taiwan FDA Registration: a1473df243fa2ea4a364538ff6543d46
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Device Details

Beckman Coulter AQUIOS Tetra-1 & Tetra-2+ Panel
TW: ่ฒๅ…‹ๆ›ผๅบซ็ˆพ็‰น่‰พ็ง‘็ˆพๆ–ฏๅ››ๅˆไธ€ๆŠ—้ซ”ๅฅ—็ต„
Risk Class 2
MD

Registration Details

a1473df243fa2ea4a364538ff6543d46

Ministry of Health Medical Device Import No. 027993

DHA05602799304

Company Information

United States

Product Details

AQUIOS Tetra-1 Panel and AQUIOS Tetra-2+ Panel single-agent antibody reagents are used in AQUIOS CL flow cytometry for cell identification and enumeration.

B Hematology and pathology devices

B5220 automatically differentiates cell counters

Imported from abroad

Dates and Status

Dec 10, 2015

Dec 10, 2025