gudid Primary ID: 332015

Plexufix (UDI 332015)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Plexufix (Model/Catalog Number: 332015) is a medical device manufactured by B. BRAUN MEDICAL INC.. This product is indexed under FDA Product Code / Category Classification BSP within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 332015
Product Code / EMDN: BSP
Device Name: Plexufix 22 Ga. x 1-1/2 in. Needle and Extension Set, 45 Bevel (Non-Insulated) (BP2215)
Database Sync Date: 2026-08-09 09:10:23

Full Regulatory Attributes

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{
    "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 Plexufix?

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

What is the Primary UDI-DI identifier for Plexufix?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 332015.

What classification code is assigned to this device?

This device is registered under product classification code BSP.

Similar Classification Devices (BSP)

Other Devices by B. BRAUN MEDICAL INC.

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