GUDIDData
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gudid Primary ID: EZPC4466

Minicap (UDI EZPC4466)

Manufactured by Vantive US Healthcare LLC

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Minicap - Primary ID EZPC4466

Device Regulatory Overview

The Minicap (Model/Catalog Number: EZPC4466) is a medical device manufactured by Vantive US Healthcare LLC. This product is indexed under FDA Product Code / Category Classification KDJ within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 1 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-0409-2026 View Full Alert →

Sharesource Connectivity Platform for Use with Homechoice Claria Product Code 5CGM01 software versions 7.13.3 (China), 8.13.2 (APAC and ...

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Technical Specifications

Model Number
EZPC4466
Product Code / EMDN
KDJ
Device Name
This device is a plastic disconnect cap for peritoneal dialysis and contains povidone-iodine intended to protect the female Luer connector of the Baxter transfer set.
Database Sync Date
2026-08-09 09:08:43

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

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Frequently Asked Questions

Who is the primary manufacturer of Minicap?

The registered manufacturer of record for Minicap is Vantive US Healthcare LLC.

What is the Primary UDI-DI identifier for Minicap?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is EZPC4466.

What classification code is assigned to this device?

This device is registered under product classification code KDJ.

Similar Classification Devices (KDJ)

Other Devices by Vantive US Healthcare LLC

Programmatic Export

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