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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 3 of 5
DeviceModel / ReferenceRegistriesClassStatus
CyFlow™ CD3 PerCP-Cy5.5 AS531857
FDA UDI
Class IActive
CyFlow™ CD13 PE AH865533
FDA UDI
Class IActive
CyFlow™ CD4 APC-Cy7 BG403070
FDA UDI
Class IActive
CyFlow™ CD15 FITC BA723310
FDA UDI
Class IActive
CyFlow™ CD16 Pacific Blue™ BV347796
FDA UDI
Class IActive
CyFlow™ CD7 PE-DyLight™ 594 AE552987
FDA UDI
Class IActive
CyFlow™ CD56 PE BH175538
FDA UDI
Class IActive
CyFlow™ CD4 PE-Cy7 CB057671
FDA UDI
Class IActive
CyFlow™ CD15 Pacific Blue™ BS022461
FDA UDI
Class IActive
CyFlow™ CD62P Biotin BN849744
FDA UDI
Class IActive
CyFlow™ CD16 Pacific Orange™ CW588602
FDA UDI
Class IActive
CyFlow™ CD16 PerCP BP172777
FDA UDI
Class IActive
CyFlow™ CD9 Pacific Blue™ CF790155
FDA UDI
Class IActive
CyFlow™ CD79a FITC AD255544
FDA UDI
Class IActive
CyFlow™ CD19 PE-Cy7 BE394220
FDA UDI
Class IActive
CyFlow™ CD71 APC-Cy7 BD471787
FDA UDI
Class IActive
CyFlow™ CD8 PE-Cy7 CN302860
FDA UDI
Class IActive
CyFlow™ CD45 PerCP-Cy5.5 CN540973
FDA UDI
Class IActive
CyFlow™ Lambda-LC APC BC500136
FDA UDI
Class IActive
CyFlow™ CD34 PE-DyLight™ 594 AW747238
FDA UDI
Class IActive
CyFlow™ CD7 PE-Cy7 AG597425
FDA UDI
Class IActive
CyFlow™ IgD PE BM781357
FDA UDI
Class IActive
CyFlow™ CD5 PE-Cy7 BZ394937
FDA UDI
Class IActive
CyFlow™ CD305 FITC BP092023
FDA UDI
Class IActive
CyFlow™ CD235a PE BJ054594
FDA UDI
Class IActive
CyFlow™ CD1a PE CY474758
FDA UDI
Class IActive
CyFlow™ Kappa-LC APC CJ989545
FDA UDI
Class IActive
CyFlow™ CD25 PE-Cy5 BS704807
FDA UDI
Class IActive
CyFlow™ CD16 FITC BM977342
FDA UDI
Class IActive
CyFlow™ CD8 PE AE526407
FDA UDI
Class IActive
CyFlow™ CD25 PE BZ199797
FDA UDI
Class IActive
CyFlow™ CD138 APC BT416655
FDA UDI
Class IActive
CyFlow™ CD19 PE-DyLight™ 594 CV284439
FDA UDI
Class IActive
CyFlow™ Lambda-LC PE AV897908
FDA UDI
Class IActive
CyFlow™ CD20 PE-Cy7 AW819478
FDA UDI
Class IActive
CyFlow™ CD10 PE-DyLight™ 594 AM327168
FDA UDI
Class IActive
CyFlow™ CD3 APC AE076656
FDA UDI
Class IActive
CyFlow™ CD2 PE-Cy7 BE056797
FDA UDI
Class IActive
CyFlow™ CD26 PE AT758612
FDA UDI
Class IActive
CyFlow™ CD23 PerCP-Cy5.5 BR282546
FDA UDI
Class IActive
CyFlow™ Lambda-LC Alexa Fluor™ 488 BA315448
FDA UDI
Class IActive
CyFlow™ CD23 PE-DyLight™ 594 BU644244
FDA UDI
Class IActive
CyFlow™ Lambda-LC FITC BL151211
FDA UDI
Class IActive
CyFlow™ CD16 PE-DyLight™ 594 BT577958
FDA UDI
Class IActive
CyFlow™ CD56 PerCP-Cy5.5 AB264380
FDA UDI
Class IActive
CyFlow™ CD34 PE-Cy7 BB415289
FDA UDI
Class IActive
CyFlow™ CD117 FITC CB916607
FDA UDI
Class IActive
CyFlow™ CD3 Pacific Orange™ BL302014
FDA UDI
Class IActive
CyFlow™ MPO APC BC667757
FDA UDI
Class IActive
CyFlow™ CD157 PE AK825233
FDA UDI
Class IActive

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