IOB (UDI IOB-029S)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The IOB (Model/Catalog Number: IOB-029S) is a medical device manufactured by Iob Medical Inc.. This product is indexed under FDA Product Code / Category Classification DWJ within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: IOB-029S
Product Code / EMDN: DWJ
Device Name
Database Sync Date: 2026-08-09 09:05:25

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 IOB?

The registered manufacturer of record for IOB is Iob Medical Inc..

What is the Primary UDI-DI identifier for IOB?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IOB-029S.

What classification code is assigned to this device?

This device is registered under product classification code DWJ.

Similar Classification Devices (DWJ)

Other Devices by Iob Medical Inc.

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