gudid Primary ID: 000281152

Ambu Immobilization Kit, with (UDI 000281152)

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: 000281152) 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: 000281152
Product Code / EMDN: IQK
Device Name: Ambu Perfit ACE and Ambu Head Wedge, Adult
Database Sync Date: 2026-08-09 09:00:28

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

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 000281152.

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

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint