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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 2 of 5
DeviceModel / ReferenceRegistriesClassStatus
CyFlow™ CD22 PerCP-Cy5.5 CJ847663
FDA UDI
Class IActive
CyFlow™ CD103 APC CY310106
FDA UDI
Class IActive
CyFlow™ CD20 APC-Cy7 BV616706
FDA UDI
Class IActive
CyFlow™ CD38 Pacific Blue™ CY054757
FDA UDI
Class IActive
CyFlow™ CD14 PE BR806060
FDA UDI
Class IActive
CyFlow™ CD11b APC-Cy7 CB102695
FDA UDI
Class IActive
CyFlow™ CD43 APC-Cy7 CS645683
FDA UDI
Class IActive
CyFlow™ CD38 PerCP-Cy5.5 AW651359
FDA UDI
Class IActive
CyFlow™ CD20 Pacific Blue™ AQ315269
FDA UDI
Class IActive
CyFlow™ CD117 APC-Cy7 AV116714
FDA UDI
Class IActive
CyFlow™ CD7 PerCP-Cy5.5 BX671123
FDA UDI
Class IActive
CyFlow™ CD30 APC BY776645
FDA UDI
Class IActive
CyFlow™ CD11c APC BA249284
FDA UDI
Class IActive
CyFlow™ CD5 FITC BP901742
FDA UDI
Class IActive
CyFlow™ CD45 Pacific Orange™ AX750746
FDA UDI
Class IActive
CyFlow™ CD8 Pacific Blue™ BL359871
FDA UDI
Class IActive
CyFlow™ CD24 APC AK914774
FDA UDI
Class IActive
CyFlow™ CD10 PE-Cy7 AL156483
FDA UDI
Class IActive
CyFlow™ CD38 APC-Cy7 CF500067
FDA UDI
Class IActive
CyFlow™ CD20 FITC CS695242
FDA UDI
Class IActive
CyFlow™ CD22 PE CY876709
FDA UDI
Class IActive
CyFlow™ CD103 FITC AP944424
FDA UDI
Class IActive
CyFlow™ CD4 FITC CX308439
FDA UDI
Class IActive
CyFlow™ CD14 Pacific Blue™ BM873624
FDA UDI
Class IActive
CyFlow™ Kappa-LC PE BL478505
FDA UDI
Class IActive
CyFlow™ CD117 PE AA189124
FDA UDI
Class IActive
CyFlow™ CD36 APC CB633121
FDA UDI
Class IActive
CyFlow™ CD3 FITC CF225414
FDA UDI
Class IActive
CyFlow™ CD11b PE-Cy7 CB652124
FDA UDI
Class IActive
CyFlow™ CD123 PE-DyLight™ 594 CD300589
FDA UDI
Class IActive
CyFlow™ Kappa-LC Alexa Fluor™ 488 BZ229827
FDA UDI
Class IActive
CyFlow™ CD123 PE AG578371
FDA UDI
Class IActive
CyFlow™ CD56 APC CK388455
FDA UDI
Class IActive
CyFlow™ CD117 PerCP-Cy5.5 AB967109
FDA UDI
Class IActive
CyFlow™ CD20 PE-DyLight™ 594 BA277544
FDA UDI
Class IActive
CyFlow™ CD79a APC BL177563
FDA UDI
Class IActive
CyFlow™ HLA-DR APC-Cy7 BT262476
FDA UDI
Class IActive
CyFlow™ CD20 PerCP-Cy5.5 AT747904
FDA UDI
Class IActive
CyFlow™ CD235a FITC AY450655
FDA UDI
Class IActive
CyFlow™ CD14 APC AJ446631
FDA UDI
Class IActive
CyFlow™ CD14 APC-Cy7 AS126181
FDA UDI
Class IActive
CyFlow™ CD8 APC AU421483
FDA UDI
Class IActive
CyFlow™ MPO PE CG673145
FDA UDI
Class IActive
CyFlow™ CD16 PE-Cy7 CB059464
FDA UDI
Class IActive
CyFlow™ CD3 PE-DyLight™ 594 BN544098
FDA UDI
Class IActive
CyFlow™ CD21 Pacific Blue™ CD048836
FDA UDI
Class IActive
CyFlow™ CD19 PE CM890606
FDA UDI
Class IActive
CyFlow™ CD11c PE-Cy7 CW003768
FDA UDI
Class IActive
CyFlow™ CD16 PE CA029636
FDA UDI
Class IActive
CyFlow™ CD8 PerCP-Cy5.5 CG526918
FDA UDI
Class IActive

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