GUDIDData
enforcement Primary ID: Z-1458-2023

Anesthesia Set Coax 180, MP03384 (UDI Z-1458-2023)

Manufactured by Draeger Medical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anesthesia Set Coax 180, MP03384 - Primary ID Z-1458-2023

Device Regulatory Overview

The Anesthesia Set Coax 180, MP03384 (Model/Catalog Number: Unspecified) is a medical device manufactured by Draeger Medical, Inc.. This product is indexed under FDA Product Code / Category Classification UDI-DI: 04048675552833; All lots. within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2753-2026 View Full Alert →

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ID: Z-2755-2026 View Full Alert →

FARADRIVE STEERABLE SHEATH CLEAR, used to facilitate access to the vasculature and into the chambers of the heart, Material Number 21M402, I...

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ID: Z-2793-2026 View Full Alert →

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🔒 Compromised Lot & Serial Numbers Locked
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Technical Specifications

Model Number
N/A
Device Name
Anesthesia Set Coax 180, MP03384
Database Sync Date
2026-08-09 10:06:34

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 Anesthesia Set Coax 180, MP03384?

The registered manufacturer of record for Anesthesia Set Coax 180, MP03384 is Draeger Medical, Inc..

What is the Primary UDI-DI identifier for Anesthesia Set Coax 180, MP03384?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z-1458-2023.

What classification code is assigned to this device?

This device is registered under product classification code UDI-DI: 04048675552833; All lots..

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