gudid Primary ID: 5064

EndoSound Biopsy Port Adapter (5 pack) 5064 (UDI 5064)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The EndoSound Biopsy Port Adapter (5 pack) 5064 (Model/Catalog Number: 5064) is a medical device manufactured by Endosound, Inc.. This product is indexed under FDA Product Code / Category Classification ODC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 5064
Product Code / EMDN: ODC
Device Name: EndoSound - Biopsy Port Adapter (5 pack) 5064 for use with compatible endoscopes and EndoSound devices
Database Sync Date: 2026-08-09 09:37:40

Full Regulatory Attributes

🔒 Token Gated

{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of EndoSound Biopsy Port Adapter (5 pack) 5064?

The registered manufacturer of record for EndoSound Biopsy Port Adapter (5 pack) 5064 is Endosound, Inc..

What is the Primary UDI-DI identifier for EndoSound Biopsy Port Adapter (5 pack) 5064?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 5064.

What classification code is assigned to this device?

This device is registered under product classification code ODC.

Similar Classification Devices (ODC)

Other Devices by Endosound, Inc.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint