GUDIDData
gudid Primary ID: 6600

Compact (UDI 6600)

Manufactured by VITALOGRAPH (IRELAND) LIMITED

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Compact - Primary ID 6600

Device Regulatory Overview

The Compact (Model/Catalog Number: 6600) is a medical device manufactured by VITALOGRAPH (IRELAND) LIMITED. This product is indexed under FDA Product Code / Category Classification BZG within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
6600
Product Code / EMDN
BZG
Device Name
GENERIC CLINICAL TRIAL CASE - MIP MEP COMPACT(1)
Database Sync Date
2026-08-09 09:22:51

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 Compact?

The registered manufacturer of record for Compact is VITALOGRAPH (IRELAND) LIMITED.

What is the Primary UDI-DI identifier for Compact?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 6600.

What classification code is assigned to this device?

This device is registered under product classification code BZG.

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