GUDIDData
gudid Primary ID: 8003032

Solus Laryngeal Mask Airway Kit, Size 3 (UDI 8003032)

Manufactured by Intersurgical Incorporated

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Solus Laryngeal Mask Airway Kit, Size 3 - Primary ID 8003032

Device Regulatory Overview

The Solus Laryngeal Mask Airway Kit, Size 3 (Model/Catalog Number: 8003032) is a medical device manufactured by Intersurgical Incorporated. This product is indexed under FDA Product Code / Category Classification CAE within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
8003032
Product Code / EMDN
CAE
Device Name
Solus Laryngeal Mask Airway Kit, Size 3
Database Sync Date
2026-08-09 09:31:32

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 Solus Laryngeal Mask Airway Kit, Size 3?

The registered manufacturer of record for Solus Laryngeal Mask Airway Kit, Size 3 is Intersurgical Incorporated.

What is the Primary UDI-DI identifier for Solus Laryngeal Mask Airway Kit, Size 3?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8003032.

What classification code is assigned to this device?

This device is registered under product classification code CAE.

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