GUDIDData
Bulk Audit Tool API Access
gudid Primary ID: 1015.054

VYGON (UDI 1015.054)

Manufactured by Vygon Corporation

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VYGON - Primary ID 1015.054

Device Regulatory Overview

The VYGON (Model/Catalog Number: 1015.054) is a medical device manufactured by Vygon Corporation. This product is indexed under FDA Product Code / Category Classification FPD 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-1802-2012 View Full Alert →

Churchill Medical Systems, Inc. A VYGON Company PICC LINE TRAY Kit Prefilled syringes included in the tray kit are used to maintain the p...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1798-2012 View Full Alert →

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 3mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syri...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-1799-2012 View Full Alert →

Vygon VY(TM)Flush Heparin Lock Flush Syringes, 10 Units per mL, 5mL in a 10mL Flush Syringe, 30 syringes per box, Rx only Prefilled syri...

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

Technical Specifications

Model Number
1015.054
Product Code / EMDN
FPD
Device Name
5ML SYRINGE FOR SAFETY CONNECTION NUTRISAFE 2 VY-P
Database Sync Date
2026-08-09 09:05:06

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of VYGON?

The registered manufacturer of record for VYGON is Vygon Corporation.

What is the Primary UDI-DI identifier for VYGON?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1015.054.

What classification code is assigned to this device?

This device is registered under product classification code FPD.

Similar Classification Devices (FPD)

Other Devices by Vygon Corporation

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint