GUDIDData
gudid Primary ID: 601241

APEX (UDI 601241)

Manufactured by B. BRAUN MEDICAL INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for APEX - Primary ID 601241

Device Regulatory Overview

The APEX (Model/Catalog Number: 601241) is a medical device manufactured by B. BRAUN MEDICAL INC.. This product is indexed under FDA Product Code / Category Classification NEP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
601241
Product Code / EMDN
NEP
Device Name
APEX LOAD CELL MODULE, EU
Database Sync Date
2026-08-09 09:43:18

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 APEX?

The registered manufacturer of record for APEX is B. BRAUN MEDICAL INC..

What is the Primary UDI-DI identifier for APEX?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 601241.

What classification code is assigned to this device?

This device is registered under product classification code NEP.

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