gudid
Primary ID: 601240
APEX (UDI 601240)
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 601240
Device Regulatory Overview
The APEX (Model/Catalog Number: 601240) 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
- 601240
- Product Code / EMDN
- NEP
- Device Name
- APEX PUMP 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
}
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 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 601240.
What classification code is assigned to this device?
This device is registered under product classification code NEP.
Similar Classification Devices (NEP)
Other Devices by B. BRAUN MEDICAL INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint