GUDIDData
Bulk Audit Tool API Access
eudamed_udi Primary ID: 07045430014954

The V-Vac Suction Unit (UDI 07045430014954)

Manufactured by Laerdal Medical AS

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for The V-Vac Suction Unit - Primary ID 07045430014954

Device Regulatory Overview

The The V-Vac Suction Unit (Model/Catalog Number: 985002) is a medical device manufactured by Laerdal Medical AS. This product is indexed under FDA Product Code / Category Classification R0580 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
985002
Product Code / EMDN
R0580
Device Name
V-VAC Manual Suction Unit
Database Sync Date
2026-08-09 16:30:10

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 The V-Vac Suction Unit?

The registered manufacturer of record for The V-Vac Suction Unit is Laerdal Medical AS.

What is the Primary UDI-DI identifier for The V-Vac Suction Unit?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07045430014954.

What classification code is assigned to this device?

This device is registered under product classification code R0580.

Similar Classification Devices (R0580)

Other Devices by Laerdal Medical AS

Programmatic Export

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

JSON API Endpoint