gudid Primary ID: 5640CEI

Vital Signs (UDI 5640CEI)

Manufactured by AIRLIFE

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Vital Signs (Model/Catalog Number: 5640CEI) is a medical device manufactured by AIRLIFE. This product is indexed under FDA Product Code / Category Classification CCK within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5640CEI
Product Code / EMDN: CCK
Device Name: Vital Signs Gas Sampling Interface
Database Sync Date: 2026-08-09 09:16:32

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 Vital Signs?

The registered manufacturer of record for Vital Signs is AIRLIFE.

What is the Primary UDI-DI identifier for Vital Signs?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5640CEI.

What classification code is assigned to this device?

This device is registered under product classification code CCK.

Similar Classification Devices (CCK)

Other Devices by AIRLIFE

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