gudid Primary ID: MP-2785-G21

MP-2785-G21 (UDI MP-2785-G21)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The MP-2785-G21 (Model/Catalog Number: MP-2785-G21) is a medical device manufactured by FUJIFILM CORPORATION. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MP-2785-G21
Product Code / EMDN: IYO
Device Name: Needle Guide
Database Sync Date: 2026-08-09 09:15:37

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 MP-2785-G21?

The registered manufacturer of record for MP-2785-G21 is FUJIFILM CORPORATION.

What is the Primary UDI-DI identifier for MP-2785-G21?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MP-2785-G21.

What classification code is assigned to this device?

This device is registered under product classification code IYO.

Similar Classification Devices (IYO)

Other Devices by FUJIFILM CORPORATION

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