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EXBIO Praha, a.s.

US

Last updated May 24, 2026

What EXBIO Praha, a.s. makes

The company manufactures in vitro diagnostic (IVD) reagents designed for identifying cell surface markers in multiple CD cell types. These products include fluorescently labeled antibodies for flow cytometry applications, such as CyFlow™ CD123 PerCP-Cy5.5 and CyFlow™ CD27 FITC, which target specific antigens like CD123 and CD27. Additional markers include CyFlow™ CD81 Alexa Fluor™ 700, CyFlow™ CD10 Alexa Fluor™ 700, and CyFlow™ Ki-67 PE, among others. These reagents are used to analyze cell populations in research and clinical diagnostics.

The portfolio consists of Class I devices, which are generally considered low-risk and subject to minimal regulatory oversight. These products are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance with U.S. regulatory requirements. The company operates from the United States, adhering to applicable IVD regulations for these diagnostic tools.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does EXBIO Praha, a.s. manufacture?

EXBIO Praha, a.s. specializes in in vitro diagnostic (IVD) reagents, specifically fluorescently labeled antibodies for flow cytometry. These products are designed to identify and analyze cell surface markers in multiple CD cell types, such as CyFlow™ CD123 PerCP-Cy5.5 or CyFlow™ CD27 FITC. These reagents help researchers and clinicians study cell populations in research and clinical diagnostics.

Where is EXBIO Praha, a.s. based, and what does that mean for its regulatory compliance?

EXBIO Praha, a.s. is based in the United States, which means its IVD products must comply with U.S. regulatory requirements. Since these devices fall under Class I classification—considered low-risk—they are subject to minimal regulatory oversight, though they are still required to meet FDA standards for safety and performance. The company’s devices are listed in the FDA’s Unique Device Identifier (UDI) database, ensuring traceability and compliance.

Which regulatory registries list EXBIO Praha, a.s.’s devices?

EXBIO Praha, a.s.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. This registry ensures that each product is traceable and meets U.S. regulatory requirements, particularly for Class I IVD reagents like their CyFlow™ antibody conjugates. Listing in the UDI database is a key compliance step for manufacturers to demonstrate regulatory adherence.

How are EXBIO Praha, a.s.’s devices classified under U.S. regulations?

EXBIO Praha, a.s.’s devices are classified as Class I in vitro diagnostics (IVDs). This classification is assigned based on risk assessment—Class I devices are generally considered low-risk and pose minimal harm to patients or users. As a result, they require minimal regulatory oversight, though they must still comply with FDA requirements for labeling, manufacturing controls, and UDI registration to ensure safety and proper use.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
sysmex.com
LinkedIn
—
Facebook
—
Phone
1-888-879-7639
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
495024965

Catalogue (236)

Page 4 of 5
DeviceModel / ReferenceRegistriesClassStatus
CyFlow™ CD10 APC AE500810
FDA UDI
Class IActive
CyFlow™ CD10 FITC AZ964070
FDA UDI
Class IActive
CyFlow™ CD3 Alexa Fluor™ 700 CR526096
FDA UDI
Class IActive
CyFlow™ Perforin PE AT934931
FDA UDI
Class IActive
CyFlow™ CD45 Pacific Blue™ AJ846005
FDA UDI
Class IActive
CyFlow™ CD14 FITC CY050198
FDA UDI
Class IActive
CyFlow™ CD138 PerCP-Cy5.5 CG044699
FDA UDI
Class IActive
CyFlow™ CD7 APC BR387152
FDA UDI
Class IActive
CyFlow™ CD13 PerCP-Cy5.5 CJ312396
FDA UDI
Class IActive
CyFlow™ CD33 FITC CB896202
FDA UDI
Class IActive
CyFlow™ CD71 PE CW883509
FDA UDI
Class IActive
CyFlow™ CD5 PerCP-Cy5.5 AJ621789
FDA UDI
Class IActive
CyFlow™ CD19 APC-Cy7 AC181482
FDA UDI
Class IActive
CyFlow™ CD33 PE CX980607
FDA UDI
Class IActive
CyFlow™ CD19 APC AG992046
FDA UDI
Class IActive
CyFlow™ CD38 PE-Cy7 AM704693
FDA UDI
Class IActive
CyFlow™ Kappa-LC FITC AU869806
FDA UDI
Class IActive
CyFlow™ CD34 FITC BU537472
FDA UDI
Class IActive
CyFlow™ CD20 APC BD786743
FDA UDI
Class IActive
CyFlow™ CD13 APC BZ475676
FDA UDI
Class IActive
CyFlow™ CD36 FITC BW219814
FDA UDI
Class IActive
CyFlow™ CD79b PE AF302547
FDA UDI
Class IActive
CyFlow™ CD19 Alexa Fluor™ 700 CQ464875
FDA UDI
Class IActive
CyFlow™ CD16 Alexa Fluor™ 700 AX355453
FDA UDI
Class IActive
CyFlow™ CD45R0 FITC BC287359
FDA UDI
Class IActive
CyFlow™ CD13 PE-DyLight™ 594 CF402545
FDA UDI
Class IActive
CyFlow™ CD8 PE-DyLight™ 594 CY194681
FDA UDI
Class IActive
CyFlow™ CD8 Pacific Orange™ AJ277511
FDA UDI
Class IActive
CyFlow™ CD2 APC AG136273
FDA UDI
Class IActive
CyFlow™ CD56 FITC BA204499
FDA UDI
Class IActive
CyFlow™ CD8 PerCP CR669071
FDA UDI
Class IActive
CyFlow™ CD34 PerCP-Cy5.5 AW446114
FDA UDI
Class IActive
CyFlow™ CD10 APC-Cy7 CB784438
FDA UDI
Class IActive
CyFlow™ CD103 PE BV476155
FDA UDI
Class IActive
CyFlow™ CD14 PE-DyLight™ 594 CP631144
FDA UDI
Class IActive
CyFlow™ CD33 APC AW821754
FDA UDI
Class IActive
CyFlow™ CD200 APC AN626647
FDA UDI
Class IActive
CyFlow™ CD13 FITC AV618426
FDA UDI
Class IActive
CyFlow™ CD33 PerCP-Cy5.5 AH247938
FDA UDI
Class IActive
CyFlow™ CD79a PE CW331549
FDA UDI
Class IActive
CyFlow™ CD4 PE CP040161
FDA UDI
Class IActive
CyFlow™ CD8 APC-Cy7 AJ592050
FDA UDI
Class IActive
CyFlow™ CD45 FITC AG109229
FDA UDI
Class IActive
CyFlow™ CD23 APC CV314141
FDA UDI
Class IActive
CyFlow™ CD57 FITC BJ224128
FDA UDI
Class IActive
CyFlow™ CD14 PerCP-Cy5.5 BH554933
FDA UDI
Class IActive
CyFlow™ CD64 Alexa Fluor™ 700 BF157637
FDA UDI
Class IActive
CyFlow™ CD16 APC BD526236
FDA UDI
Class IActive
CyFlow™ CD138 FITC AP577217
FDA UDI
Class IActive
CyFlow™ CD2 FITC BL464856
FDA UDI
Class IActive

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