gudid Primary ID: MAJ-1218

SINGLE USE BIOPSY VALVE (UDI MAJ-1218)

Manufactured by OLYMPUS MEDICAL SYSTEMS CORP.

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

Scannable UDI-DI Representation

Device Regulatory Overview

The SINGLE USE BIOPSY VALVE (Model/Catalog Number: MAJ-1218) is a medical device manufactured by OLYMPUS MEDICAL SYSTEMS CORP.. This product is indexed under FDA Product Code / Category Classification EOB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: MAJ-1218
Product Code / EMDN: EOB
Device Name: SINGLE USE BIOPSY VALVE MAJ-1218
Database Sync Date: 2026-08-09 09:29:18

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 SINGLE USE BIOPSY VALVE?

The registered manufacturer of record for SINGLE USE BIOPSY VALVE is OLYMPUS MEDICAL SYSTEMS CORP..

What is the Primary UDI-DI identifier for SINGLE USE BIOPSY VALVE?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MAJ-1218.

What classification code is assigned to this device?

This device is registered under product classification code EOB.

Similar Classification Devices (EOB)

Other Devices by OLYMPUS MEDICAL SYSTEMS CORP.

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