gudid Primary ID: 000281153

Ambu Immobilization Kit, with (UDI 000281153)

Manufactured by Ambu A/S

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Ambu Immobilization Kit, with (Model/Catalog Number: 000281153) is a medical device manufactured by Ambu A/S. This product is indexed under FDA Product Code / Category Classification IQK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 000281153
Product Code / EMDN: IQK
Device Name: Ambu Military Perfit ACE and Ambu Military Head Wedge, Adult
Database Sync Date: 2026-08-09 09:00:28

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 Ambu Immobilization Kit, with?

The registered manufacturer of record for Ambu Immobilization Kit, with is Ambu A/S.

What is the Primary UDI-DI identifier for Ambu Immobilization Kit, with?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000281153.

What classification code is assigned to this device?

This device is registered under product classification code IQK.

Similar Classification Devices (IQK)

Other Devices by Ambu A/S

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