GUDIDData
eudamed_udi Primary ID: 05051986013619

LogiTube Lux Illuminated Gastric Calibration Tube (UDI 05051986013619)

Manufactured by Surgical Innovations Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LogiTube Lux Illuminated Gastric Calibration Tube - Primary ID 05051986013619

Device Regulatory Overview

The LogiTube Lux Illuminated Gastric Calibration Tube (Model/Catalog Number: 36LUXTUBEB) is a medical device manufactured by Surgical Innovations Ltd.. This product is indexed under FDA Product Code / Category Classification G020502 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
36LUXTUBEB
Product Code / EMDN
G020502
Device Name
LogiTube Gastric Calibration Tube
Database Sync Date
2026-08-09 16:47:00

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 LogiTube Lux Illuminated Gastric Calibration Tube?

The registered manufacturer of record for LogiTube Lux Illuminated Gastric Calibration Tube is Surgical Innovations Ltd..

What is the Primary UDI-DI identifier for LogiTube Lux Illuminated Gastric Calibration Tube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05051986013619.

What classification code is assigned to this device?

This device is registered under product classification code G020502.

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