eudamed_udi Primary ID: 05407008321192

Scoot Control SUBD9 (UDI 05407008321192)

Manufactured by mo-vis bv

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Scoot Control SUBD9 (Model/Catalog Number: P015-81) is a medical device manufactured by mo-vis bv. This product is indexed under FDA Product Code / Category Classification Y122403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: P015-81
Product Code / EMDN: Y122403
Device Name: Scoot Control
Database Sync Date: 2026-08-09 16:28:56

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 Scoot Control SUBD9?

The registered manufacturer of record for Scoot Control SUBD9 is mo-vis bv.

What is the Primary UDI-DI identifier for Scoot Control SUBD9?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05407008321192.

What classification code is assigned to this device?

This device is registered under product classification code Y122403.

Similar Classification Devices (Y122403)

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