GUDIDData
eudamed_udi Primary ID: 10889483603352

Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector  (UDI 10889483603352)

Manufactured by AirLife Finland Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector  - Primary ID 10889483603352

Device Regulatory Overview

The Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector  (Model/Catalog Number: M1154610) is a medical device manufactured by AirLife Finland Oy. This product is indexed under FDA Product Code / Category Classification R020301 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
M1154610
Product Code / EMDN
R020301
Device Name
Vital Signs™ Respiratory Circuits Connection Pipes
Database Sync Date
2026-08-09 16:28:52

Full Regulatory Attributes

🔒 Token Gated
{
    "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™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector ?

The registered manufacturer of record for Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector  is AirLife Finland Oy.

What is the Primary UDI-DI identifier for Vital Signs™ Manual Ventilation Tube for ABS Bag Arm, Expandable, Disposable, 1.8 m/72 in With ABS Bag Arm Connector ?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10889483603352.

What classification code is assigned to this device?

This device is registered under product classification code R020301.

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