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Pendracare International, B.V.

US

Last updated May 27, 2026

What Pendracare International, B.V. makes

Pendracare International manufactures single-use vascular guide-catheters and urodynamic catheters, designed for procedural and diagnostic applications in vascular and urological settings.

The company’s products are classified as Class II devices and are listed in the FDA’s Unique Device Identifier (UDI) database, adhering to U.S. regulatory requirements.

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 Pendracare International, B.V. manufacture?

Pendracare International, B.V. specializes in single-use medical devices, specifically vascular guide-catheters and urodynamic catheters. These devices are designed for use in vascular and urological procedures, including both diagnostic and interventional applications. The company’s focus on single-use products ensures compliance with procedural hygiene standards.

Where is Pendracare International, B.V. based, and does this affect its regulatory compliance?

Pendracare International, B.V. is based in the United States, which means its devices must comply with U.S. regulatory requirements. The company’s products are listed in the FDA’s Unique Device Identifier (UDI) database, demonstrating adherence to U.S. regulatory standards for medical devices. This listing helps ensure traceability and transparency in the supply chain.

Which regulatory registries or databases list Pendracare International’s devices?

Pendracare International’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system is a global standard for identifying medical devices, ensuring accurate tracking and regulatory compliance. Listing in this database is particularly relevant for Class II devices, which require additional scrutiny due to their moderate risk.

How are Pendracare International’s devices classified under U.S. regulations?

Pendracare International’s devices are classified as Class II under U.S. regulations. This classification is based on their intended use and associated risks—vascular guide-catheters and urodynamic catheters fall into this category because they pose moderate risks and require special controls to ensure safety and effectiveness. Class II devices undergo additional review processes to validate their performance and compliance.

Why does it matter that Pendracare International’s devices are listed in the FDA’s UDI database?

Listing in the FDA’s UDI database is critical because it provides a standardized way to identify and track medical devices throughout their lifecycle, from manufacturing to patient use. This system enhances transparency, reduces medical errors, and supports regulatory oversight. For Class II devices like those made by Pendracare International, the UDI ensures that healthcare providers and regulators can quickly access accurate information about the device’s specifications, compliance status, and potential recalls.

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

Information

Country
US
Address
—
Website
xx.xx
LinkedIn
—
Facebook
—
Phone
888-272-1001
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
413008652

Catalogue (539)

Page 6 of 11
DeviceModel / ReferenceRegistriesClassStatus
Convey 8F Convey AL1.5 SH
FDA UDI
Class IIActive
Convey 7F Convey LeftBU4.5 SH
FDA UDI
Class IIActive
Convey 7F Convey LeftBU3 SH
FDA UDI
Class IIActive
Convey 8F Convey FCL3 SH
FDA UDI
Class IIActive
Convey 6FConvey AL3
FDA UDI
Class IIActive
Convey 7F Convey FCL4.5
FDA UDI
Class IIActive
Convey 8F Convey FR3
FDA UDI
Class IIActive
Convey 7F Convey LeftBU4.25
FDA UDI
Class IIActive
Convey 5FConvey RBR4
FDA UDI
Class IIActive
Convey 7F Convey JR4.5 SH
FDA UDI
Class IIActive
Convey 6FConvey TIG5
FDA UDI
Class IIActive
Convey 6FConvey ART4.5 SH
FDA UDI
Class IIActive
Convey 6FConvey JR6
FDA UDI
Class IIActive
Convey 7F Convey ART3.75
FDA UDI
Class IIActive
Convey 8F Convey JR3
FDA UDI
Class IIActive
Convey 8F Convey LeftBU3
FDA UDI
Class IIActive
Convey 7F Convey JR3.5 SH
FDA UDI
Class IIActive
Convey 8F Convey FCL3
FDA UDI
Class IIActive
Convey 7F Convey ART4 SH
FDA UDI
Class IIActive
Convey 8F Convey LeftBU4.5 SH
FDA UDI
Class IIActive
Convey 6FConvey RC3.5SC
FDA UDI
Class IIActive
Convey 6FConvey AR2
FDA UDI
Class IIActive
Convey 8F Convey FR6
FDA UDI
Class IIActive
Convey 5FConvey FL5
FDA UDI
Class IIActive
Convey 7F Convey FL3.5 SH
FDA UDI
Class IIActive
Convey 7F Convey LCB SH
FDA UDI
Class IIActive
Convey 6FConvey KIMNY
FDA UDI
Class IIActive
Convey 8F Convey CLS4.25 SH
FDA UDI
Class IIActive
Convey 8F Convey ART3.75 SH
FDA UDI
Class IIActive
Convey 7F Convey CLS3.25 SH
FDA UDI
Class IIActive
Convey 5FConvey TIG5
FDA UDI
Class IIActive
Convey 5FConvey FL3
FDA UDI
Class IIActive
Convey 6FConvey RBR3.5 SH
FDA UDI
Class IIActive
Convey 8F Convey JL4 SH
FDA UDI
Class IIActive
Convey 7F Convey RBR3.5 SH
FDA UDI
Class IIActive
Convey 7F Convey RBL4.5
FDA UDI
Class IIActive
Convey 7F Convey ART4.5 SH
FDA UDI
Class IIActive
Convey 5FConvey FCL4.5
FDA UDI
Class IIActive
Convey 6FConvey ART4.25 SH
FDA UDI
Class IIActive
Convey 7F Convey JL3.5
FDA UDI
Class IIActive
Convey 6FConvey CLS3.25
FDA UDI
Class IIActive
Convey 7F Convey JL3.5 SH
FDA UDI
Class IIActive
Convey 5FConvey CLS3.75
FDA UDI
Class IIActive
Convey 6FConvey RBL3.5 SH
FDA UDI
Class IIActive
Convey 8F Convey LCB SH
FDA UDI
Class IIActive
Convey 6FConvey JR4.5 SH
FDA UDI
Class IIActive
Convey 8F Convey ART4
FDA UDI
Class IIActive
Convey 7F Convey RBR4 SH
FDA UDI
Class IIActive
Convey 6FConvey CLS3.75 SH
FDA UDI
Class IIActive
Convey 6FConvey AL.75
FDA UDI
Class IIActive

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