gudid Primary ID: DCA+225-25

Citric Complete (UDI DCA+225-25)

Manufactured by NIPRO RENAL SOLUTIONS USA CORPORATION

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Citric Complete (Model/Catalog Number: DCA+225-25) is a medical device manufactured by NIPRO RENAL SOLUTIONS USA CORPORATION. This product is indexed under FDA Product Code / Category Classification KPO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: DCA+225-25
Product Code / EMDN: KPO
Device Name: Dry Citric Acid Concentrate
Database Sync Date: 2026-08-09 09:31:19

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 Citric Complete?

The registered manufacturer of record for Citric Complete is NIPRO RENAL SOLUTIONS USA CORPORATION.

What is the Primary UDI-DI identifier for Citric Complete?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is DCA+225-25.

What classification code is assigned to this device?

This device is registered under product classification code KPO.

Similar Classification Devices (KPO)

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