eudamed_udi Primary ID: 08720618074034

Kinetic Balance (UDI 08720618074034)

Manufactured by Positioning Products B.V.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Kinetic Balance (Model/Catalog Number: 5.70002.3 - Chest Harness Stretch X-shape / L) is a medical device manufactured by Positioning Products B.V.. This product is indexed under FDA Product Code / Category Classification Y180980 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5.70002.3 - Chest Harness Stretch X-shape / L
Product Code / EMDN: Y180980
Device Name: Positioning Products
Database Sync Date: 2026-08-09 16:44:57

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 Kinetic Balance?

The registered manufacturer of record for Kinetic Balance is Positioning Products B.V..

What is the Primary UDI-DI identifier for Kinetic Balance?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720618074034.

What classification code is assigned to this device?

This device is registered under product classification code Y180980.

Similar Classification Devices (Y180980)

Other Devices by Positioning Products B.V.

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