GUDIDData
gudid Primary ID: VP-7000

FUJIFILM (UDI VP-7000)

Manufactured by FUJIFILM CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for FUJIFILM - Primary ID VP-7000

Device Regulatory Overview

The FUJIFILM (Model/Catalog Number: VP-7000) is a medical device manufactured by FUJIFILM CORPORATION. This product is indexed under FDA Product Code / Category Classification PEA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
VP-7000
Product Code / EMDN
PEA
Device Name
The VP-7000 unit is used for endoscopic observation, diagnosis, treatment, and image recording. It is intended to process electronic signals transmitted from a video endoscope (a video camera in an endoscope). This product may be used on all patients requiring endoscopic examination and when using a Fujinon/FUJIFILM medical endoscope and light source together with monitor, recorder and various peripheral devices. BLI (Blue Light Imaging), LCI (Linked Color Imaging) and FICE (Flexible spectral-Imaging Color Enhancement) are adjunctive tools for gastrointestinal endoscopic examination which can be used to supplement Fujifilm white light endoscopy. BLI, LCI and FICE are not intended to replace histopathological sampling as a means of diagnosis.
Database Sync Date
2026-08-09 09:53:07

Full Regulatory Attributes

🔒 Token Gated
{
    "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 FUJIFILM?

The registered manufacturer of record for FUJIFILM is FUJIFILM CORPORATION.

What is the Primary UDI-DI identifier for FUJIFILM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is VP-7000.

What classification code is assigned to this device?

This device is registered under product classification code PEA.

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