GUDIDData
eudamed_udi Primary ID: 14026704196880

Rusch Tracheopart Tracheostomy tube set (left) (UDI 14026704196880)

Manufactured by Teleflex Medical

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Rusch Tracheopart Tracheostomy tube set (left) - Primary ID 14026704196880

Device Regulatory Overview

The Rusch Tracheopart Tracheostomy tube set (left) (Model/Catalog Number: 116400-000950) is a medical device manufactured by Teleflex Medical. This product is indexed under FDA Product Code / Category Classification R01040203 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-0675-2017 View Full Alert →

ARROW OnControl Bone Marrow Biopsy System Tray, Sterile, Rx only, Manufactured for: Teleflex Medical, The Arrow OnControl Bone Marrow Asp...

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

🔒 Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2108-2017 View Full Alert →

WECK Visistat 35R Disposable Skin Stapler, Ref 528135, Rx Only, Sterile EO, Visistat is indicated for the external skin closure of lacera...

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

Technical Specifications

Model Number
116400-000950
Product Code / EMDN
R01040203
Device Name
TRACHEOPART DOUBLE LUMEN TUBE LEFT
Database Sync Date
2026-08-09 16:58:12

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 Rusch Tracheopart Tracheostomy tube set (left)?

The registered manufacturer of record for Rusch Tracheopart Tracheostomy tube set (left) is Teleflex Medical.

What is the Primary UDI-DI identifier for Rusch Tracheopart Tracheostomy tube set (left)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 14026704196880.

What classification code is assigned to this device?

This device is registered under product classification code R01040203.

Programmatic Export

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

JSON API Endpoint