PleurX 50-7290

GUDID 50885403193543

PleurX Procedure Pack

CAREFUSION 2200, INC

Pleural/peritoneal drainage catheterization kit

• Primary Device ID: 50885403193543
• NIH Device Record Key: d39dfc65-a350-457c-884f-b7ae57ef6cdf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PleurX
• Version Model Number: 50-7290
• Catalog Number: 50-7290
• Company DUNS: 832696038
• Company Name: CAREFUSION 2200, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)323-9088
• Email: gmb-MedSpec-CustService@carefusion.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com
• Phone: +1(800)323-9088
• Email: Customer_Support@BD.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885403193545 [Primary]
GS1	50885403193543 [Package]; Contains: 10885403193545; Package: Case [5 Units]; In Commercial Distribution

FDA Product Code

• DWM: Apparatus, Suction, Patient Care

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-11-13
• Device Publish Date: 2017-06-12

On-Brand Devices [PleurX]

• 10885403273773: PleurX Patient Starter Kit, For Patient Home Use - 1000 ml
• 50885403090729: PleurX Vacuum Bottle - Vacuum Bottle with Drainage Line 500ml
• 50885403174870: PleurX Lockable Drainage Line
• 50885403185197: PleurX Lockable Drainage Line Kit
• 50885403090712: PleurX Drainage Kit, 500 ml
• 50885403075979: PleurX Pleural Catheter Kit, For Pleural Placement 15.5 Fr
• 10885403231537: PleurX Peritoneal Catheter and Starter Kit - For Peritoneal Placement Only and For Patient Home
• 50885403231528: PleurX Pleural Catheter and Starter Kit - For Pleural Placement Only and For Patient Home Use
• 50885403193543: PleurX Procedure Pack
• 50885403193024: PleurX Supplemental Insertion Kit
• 50885403185692: PleurX Catheter Access Kit
• 50885403090705: PleurX Drainage Kit 1000 ml (Procedure Pack)
• 50885403090682: PleurX Valve Cap
• 50885403090668: PleurX Vacuum Bottle 1000ml - Vacuum Bottle with Drainage Line
• 50885403075955: PleurX Peritoneal Catheter Kit, For Peritoneal Placement, 15.5 Fr
• 50885403075986: PleurX Pleural Catheter Mini Kit
• 50885403420526: PleurX Valve Kit