GUDIDData
gudid Primary ID: 415079

Safsite (UDI 415079)

Manufactured by B. BRAUN MEDICAL INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Safsite - Primary ID 415079

Device Regulatory Overview

The Safsite (Model/Catalog Number: 415079) is a medical device manufactured by B. BRAUN MEDICAL INC.. This product is indexed under FDA Product Code / Category Classification FPA within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
415079
Product Code / EMDN
FPA
Device Name
AP2500 ACCESS PIN W/ VALVE
Database Sync Date
2026-08-09 09:10:23

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 Safsite?

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

What is the Primary UDI-DI identifier for Safsite?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 415079.

What classification code is assigned to this device?

This device is registered under product classification code FPA.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint