gudid
Primary ID: 50-7290A
N/A (UDI 50-7290A)
Manufactured by CAREFUSION 2200, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for N/A - Primary ID 50-7290A
Device Regulatory Overview
The N/A (Model/Catalog Number: 50-7290A) 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
- 50-7290A
- Product Code / EMDN
- DWM
- Device Name
- Procedure Pack, For use with the PleurX or PeritX Catheter Systems
- Database Sync Date
- 2026-08-09 09:16:31
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of N/A?
The registered manufacturer of record for N/A is CAREFUSION 2200, INC.
What is the Primary UDI-DI identifier for N/A?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50-7290A.
What classification code is assigned to this device?
This device is registered under product classification code DWM.
Similar Classification Devices (DWM)
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