curaplex (UDI 472003000)

Manufactured by Ambu A/S

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

Scannable UDI-DI Representation

Device Regulatory Overview

The curaplex (Model/Catalog Number: 472003000) 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: 472003000
Product Code / EMDN: IQK
Device Name: Adult Adjustable Cervical Collar
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 curaplex?

The registered manufacturer of record for curaplex is Ambu A/S.

What is the Primary UDI-DI identifier for curaplex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 472003000.

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