gudid
Primary ID: BAT3018
Jamshidi (UDI BAT3018)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Jamshidi - Primary ID BAT3018
Device Regulatory Overview
The Jamshidi (Model/Catalog Number: BAT3018) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification LWE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BAT3018
- Product Code / EMDN
- LWE
- Device Name
- ILLINOIS (TIN) BONE MARROW TRAY 18G X 3
- Database Sync Date
- 2026-08-09 10:00:52
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 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 BAT3018.
What classification code is assigned to this device?
This device is registered under product classification code LWE.
Similar Classification Devices (LWE)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint