gudid Primary ID: 905-00037-E

buddy 2 SYSTEM (UDI 905-00037-E)

Manufactured by BELMONT INSTRUMENT CORPORATION

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

Scannable UDI-DI Representation

Device Regulatory Overview

The buddy 2 SYSTEM (Model/Catalog Number: 905-00037-E) is a medical device manufactured by BELMONT INSTRUMENT CORPORATION. This product is indexed under FDA Product Code / Category Classification BSB within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 905-00037-E
Product Code / EMDN: BSB
Device Name: BUDDY 2 SYSTEM, ENGLISH
Database Sync Date: 2026-08-09 09:46:58

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 buddy 2 SYSTEM?

The registered manufacturer of record for buddy 2 SYSTEM is BELMONT INSTRUMENT CORPORATION.

What is the Primary UDI-DI identifier for buddy 2 SYSTEM?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 905-00037-E.

What classification code is assigned to this device?

This device is registered under product classification code BSB.

Similar Classification Devices (BSB)

Other Devices by BELMONT INSTRUMENT CORPORATION

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