GUDIDData
gudid Primary ID: H938099

REPEATER (UDI H938099)

Manufactured by BAXTER HEALTHCARE CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REPEATER - Primary ID H938099

Device Regulatory Overview

The REPEATER (Model/Catalog Number: H938099) is a medical device manufactured by BAXTER HEALTHCARE CORPORATION. This product is indexed under FDA Product Code / Category Classification NEP within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 2 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2174-2021 View Full Alert →

Kaguya Automated Peritoneal Dialysis System...

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ID: Z-2173-2021 View Full Alert →

Sharesource Connectivity Platform for Use with the Amia Automated PD System...

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Technical Specifications

Model Number
H938099
Product Code / EMDN
NEP
Device Name
REPEATER Pump, Fluid Transfer Pump
Database Sync Date
2026-08-09 09:08:43

Full Regulatory Attributes

🔒 Token Gated
{
    "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 REPEATER?

The registered manufacturer of record for REPEATER is BAXTER HEALTHCARE CORPORATION.

What is the Primary UDI-DI identifier for REPEATER?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is H938099.

What classification code is assigned to this device?

This device is registered under product classification code NEP.

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