gudid Primary ID: 8050RTUC

RediTube (UDI 8050RTUC)

Manufactured by AIRLIFE

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The RediTube (Model/Catalog Number: 8050RTUC) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification BTR within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 8050RTUC
Product Code / EMDN: BTR
Device Name: Tracheal Tube Oral/Nasal with Pre-loaded Stylet
Database Sync Date: 2026-08-09 09:16:32

Full Regulatory Attributes

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{
    "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 RediTube?

The registered manufacturer of record for RediTube is AIRLIFE.

What is the Primary UDI-DI identifier for RediTube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8050RTUC.

What classification code is assigned to this device?

This device is registered under product classification code BTR.

Similar Classification Devices (BTR)

Other Devices by AIRLIFE

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