Jimini (UDI D-JiminiAZ)

Manufactured by Usense

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Jimini (Model/Catalog Number: Jimini) is a medical device manufactured by Usense. This product is indexed under FDA Product Code / Category Classification W02079099 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Jimini
Product Code / EMDN: W02079099
Device Name: Jimini
Database Sync Date: 2026-08-09 17:11:10

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 Jimini?

The registered manufacturer of record for Jimini is Usense.

What is the Primary UDI-DI identifier for Jimini?

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

What classification code is assigned to this device?

This device is registered under product classification code W02079099.

Similar Classification Devices (W02079099)

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