eudamed_udi Primary ID: 07630318406107

Jimmy (UDI 07630318406107)

Manufactured by OBA AG

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Jimmy (Model/Catalog Number: 3060.302) is a medical device manufactured by OBA AG. This product is indexed under FDA Product Code / Category Classification V080302 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 3060.302
Product Code / EMDN: V080302
Device Name: Positionierungshilfen
Database Sync Date: 2026-08-09 16:28:44

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 Jimmy?

The registered manufacturer of record for Jimmy is OBA AG.

What is the Primary UDI-DI identifier for Jimmy?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 07630318406107.

What classification code is assigned to this device?

This device is registered under product classification code V080302.

Similar Classification Devices (V080302)

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