eudamed_udi Primary ID: 05430002911106

CoMoveIT Flex (UDI 05430002911106)

Manufactured by CoMoveIT

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CoMoveIT Flex (Model/Catalog Number: CoMoveIT Flex) is a medical device manufactured by CoMoveIT. This product is indexed under FDA Product Code / Category Classification Y122403 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: CoMoveIT Flex
Product Code / EMDN: Y122403
Device Name: CoMoveIT Flex
Database Sync Date: 2026-08-09 16:30:06

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 CoMoveIT Flex?

The registered manufacturer of record for CoMoveIT Flex is CoMoveIT.

What is the Primary UDI-DI identifier for CoMoveIT Flex?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05430002911106.

What classification code is assigned to this device?

This device is registered under product classification code Y122403.

Similar Classification Devices (Y122403)

Other Devices by CoMoveIT

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