GUDIDData
gudid Primary ID: 403-00413

buddy 2 Power Module (UDI 403-00413)

Manufactured by BELMONT INSTRUMENT CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for buddy 2 Power Module - Primary ID 403-00413

Device Regulatory Overview

The buddy 2 Power Module (Model/Catalog Number: 403-00413) 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
403-00413
Product Code / EMDN
BSB
Device Name
Assy, buddy 2, Power Module, Unit
Database Sync Date
2026-08-09 09:46:58

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 buddy 2 Power Module?

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

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

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 403-00413.

What classification code is assigned to this device?

This device is registered under product classification code BSB.

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