GUDIDData
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eudamed_udi Primary ID: 14026704720375

Rüsch PVC Nasopharyngeal Airway (UDI 14026704720375)

Manufactured by Teleflex Medical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rüsch PVC Nasopharyngeal Airway - Primary ID 14026704720375

Device Regulatory Overview

The Rüsch PVC Nasopharyngeal Airway (Model/Catalog Number: 125410-000260) is a medical device manufactured by Teleflex Medical. This product is indexed under FDA Product Code / Category Classification R010101 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.

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ID: Z-1534-2014 View Full Alert →

CAPIO, Monodeck, Violet Monofilament Polydioxanone Suture, 1 x 48 inches (122cm) Absorbable Surgical Suture, Rx Only, Teleflex Medical. Pr...

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ID: Z-2108-2017 View Full Alert →

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

Technical Specifications

Model Number
125410-000260
Product Code / EMDN
R010101
Device Name
Nasopharyngeal Airway
Database Sync Date
2026-08-09 16:29:44

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 Rüsch PVC Nasopharyngeal Airway?

The registered manufacturer of record for Rüsch PVC Nasopharyngeal Airway is Teleflex Medical.

What is the Primary UDI-DI identifier for Rüsch PVC Nasopharyngeal Airway?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14026704720375.

What classification code is assigned to this device?

This device is registered under product classification code R010101.

Similar Classification Devices (R010101)

Other Devices by Teleflex Medical

Programmatic Export

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