gudid Primary ID: 8803030

I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US) (UDI 8803030)

Manufactured by Intersurgical Incorporated

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

Scannable UDI-DI Representation

Device Regulatory Overview

The I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US) (Model/Catalog Number: 8803030) 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: 8803030
Product Code / EMDN: CAE
Device Name: I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US)
Database Sync Date: 2026-08-09 09:45:58

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 I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US)?

The registered manufacturer of record for I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US) is Intersurgical Incorporated.

What is the Primary UDI-DI identifier for I-GEL PLUS RESUS PACK, SMALL ADULT, 30-60KG (US)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 8803030.

What classification code is assigned to this device?

This device is registered under product classification code CAE.

Similar Classification Devices (CAE)

Other Devices by Intersurgical Incorporated

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