GUDIDData
gudid Primary ID: 27671-001

Vmax (UDI 27671-001)

Manufactured by Carefusion Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vmax - Primary ID 27671-001

Device Regulatory Overview

The Vmax (Model/Catalog Number: 27671-001) is a medical device manufactured by Carefusion Corporation. This product is indexed under FDA Product Code / Category Classification BTY 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-1112-2013 View Full Alert →

Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and powe...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-1098-2013 View Full Alert →

Alaris PC unit model 8015 with software version 9.12 Product Usage: The Alaris PC unit is the central programming, monitoring and power ...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
27671-001
Product Code / EMDN
BTY
Device Name
KIT SWR VMAX ENCORE 27-3D
Database Sync Date
2026-08-09 09:59:02

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 Vmax?

The registered manufacturer of record for Vmax is Carefusion Corporation.

What is the Primary UDI-DI identifier for Vmax?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 27671-001.

What classification code is assigned to this device?

This device is registered under product classification code BTY.

Programmatic Export

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