GUDIDData
gudid Primary ID: NEO6

Reusable ENFit Syringe (UDI NEO6)

Manufactured by Avanos Medical, Inc.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Reusable ENFit Syringe - Primary ID NEO6

Device Regulatory Overview

The Reusable ENFit Syringe (Model/Catalog Number: NEO6) is a medical device manufactured by Avanos Medical, Inc.. This product is indexed under FDA Product Code / Category Classification PNR 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-2343-2026 View Full Alert →

Product Name: MIC Safety Percutaneous Endoscopic Gastrostomy PEG Kit 24 Fr PUSH OTW Model/Catalog Number: 7170-24 Product Description: F...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
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ID: Z-2335-2026 View Full Alert →

Product Name: CORFLO* Safety PEG Kit Model/Catalog Number: 30-6312...

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2337-2026 View Full Alert →

Product Name: CORFLO* Safety PEG Kit with ENFit Connector Model/Catalog Number: 50-4320...

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

Technical Specifications

Model Number
NEO6
Product Code / EMDN
PNR
Device Name
6mL NC at Home ENFit Syringe Reusable
Database Sync Date
2026-08-09 09:20:10

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 Reusable ENFit Syringe?

The registered manufacturer of record for Reusable ENFit Syringe is Avanos Medical, Inc..

What is the Primary UDI-DI identifier for Reusable ENFit Syringe?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is NEO6.

What classification code is assigned to this device?

This device is registered under product classification code PNR.

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