gudid
Primary ID: 50-0071
PleurX (UDI 50-0071)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PleurX - Primary ID 50-0071
Device Regulatory Overview
The PleurX (Model/Catalog Number: 50-0071) is a medical device manufactured by CAREFUSION 2200, INC. This product is indexed under FDA Product Code / Category Classification DWM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 50-0071
- Product Code / EMDN
- DWM
- Device Name
- PleurX Patient Starter Kit, For Patient Home Use - 1000 ml
- Database Sync Date
- 2026-08-09 09:16:32
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 PleurX?
The registered manufacturer of record for PleurX is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for PleurX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50-0071.
What classification code is assigned to this device?
This device is registered under product classification code DWM.
Similar Classification Devices (DWM)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint