gudid Primary ID: BEJS3411

Jamshidi (UDI BEJS3411)

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

Scannable UDI-DI Representation

Device Regulatory Overview

The Jamshidi (Model/Catalog Number: BEJS3411) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification KNW within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: BEJS3411
Product Code / EMDN: KNW
Device Name: Jamshidi Evolve Bone Marrow Biopsy Tray - 11G x 4" EJ Biopsy/Aspiration Needle with Marrow Acquisition Cradle
Database Sync Date: 2026-08-09 09:16:32

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 Jamshidi?

The registered manufacturer of record for Jamshidi is CAREFUSION 2200, INC.

What is the Primary UDI-DI identifier for Jamshidi?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BEJS3411.

What classification code is assigned to this device?

This device is registered under product classification code KNW.

Similar Classification Devices (KNW)

Other Devices by CAREFUSION 2200, INC

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