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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 3 of 11
DeviceModel / ReferenceRegistriesClassStatus
Convey 7F Convey LeftBU5
FDA UDI
Class IIActive
Convey 8F Convey ART4.5 SH
FDA UDI
Class IIActive
Convey 7F Convey JL3 SH
FDA UDI
Class IIActive
Convey 6FConvey FCL4 SH
FDA UDI
Class IIActive
Convey 6FConvey FCL4
FDA UDI
Class IIActive
Convey 6FConvey RCB
FDA UDI
Class IIActive
Convey 6FConvey JL5
FDA UDI
Class IIActive
Convey 6F Convey TIG4 SH
FDA UDI
Class IIActive
Convey 5FConvey KIMNY
FDA UDI
Class IIActive
Convey 6F Convey TIG4.5 SH
FDA UDI
Class IIActive
Convey 7F Convey LeftBU4.5
FDA UDI
Class IIActive
Convey 8F Convey JR4 SH
FDA UDI
Class IIActive
Convey 6FConvey FCL5 SH
FDA UDI
Class IIActive
Convey 8F Convey FR3.5 SH
FDA UDI
Class IIActive
Convey 7F Convey HS
FDA UDI
Class IIActive
Convey 5FConvey AL1.5
FDA UDI
Class IIActive
Convey 8F Convey CLS4.5
FDA UDI
Class IIActive
Convey 8F Convey FR4 SH
FDA UDI
Class IIActive
Convey 6FConvey CLS4.5
FDA UDI
Class IIActive
Convey 7F Convey JL6
FDA UDI
Class IIActive
Convey 7F Convey TIG4
FDA UDI
Class IIActive
Convey 7F Convey RC3.5 SC SH
FDA UDI
Class IIActive
Convey 7F Convey CLS4.25 SH
FDA UDI
Class IIActive
Convey 5FConvey ART3
FDA UDI
Class IIActive
Convey 5FConvey HS
FDA UDI
Class IIActive
Convey 6FConvey IM SH
FDA UDI
Class IIActive
Convey 5FConvey RC5SC
FDA UDI
Class IIActive
Convey 5FConvey ART4.5
FDA UDI
Class IIActive
Convey 8F Convey AR1 SH
FDA UDI
Class IIActive
Convey 6FConvey FCL3.5 SH
FDA UDI
Class IIActive
Convey 6F Convey TIG5 SH
FDA UDI
Class IIActive
Convey 7F Convey FR5
FDA UDI
Class IIActive
Convey 6FConvey JL6 SH
FDA UDI
Class IIActive
Convey 6FConvey FR5 SH
FDA UDI
Class IIActive
Convey 5FConvey JR4.5
FDA UDI
Class IIActive
Convey 5FConvey RC4SC
FDA UDI
Class IIActive
Convey 6FConvey JL4
FDA UDI
Class IIActive
Convey 8F Convey FR4.5 SH
FDA UDI
Class IIActive
Convey 5FConvey JL5
FDA UDI
Class IIActive
Convey 5FConvey FR4.5
FDA UDI
Class IIActive
Convey 6FConvey ART3
FDA UDI
Class IIActive
Convey 8F Convey AL3 SH
FDA UDI
Class IIActive
Convey 5FConvey RBR3.5
FDA UDI
Class IIActive
Convey 6FConvey FL4 SH
FDA UDI
Class IIActive
Convey 7F Convey RC4 SC
FDA UDI
Class IIActive
Convey 7F Convey TIG5 SH
FDA UDI
Class IIActive
Convey 6FConvey RC4SC
FDA UDI
Class IIActive
Convey 6FConvey FCL4.5
FDA UDI
Class IIActive
Convey 8F Convey FCL4.5 SH
FDA UDI
Class IIActive
Convey 7F Convey ART3.75 SH
FDA UDI
Class IIActive

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