4420

GUDID 50885403142183

Wet PVP-I Small Procedure Preoperative Skin Prep Tray

CAREFUSION 2200, INC

Surgical patient preparation kit

• Primary Device ID: 50885403142183
• NIH Device Record Key: 96f19f7f-55b4-45d0-8d5e-ab9ebc3f4d5c
• Commercial Distribution Discontinuation: 2023-04-30
• Commercial Distribution Status: Not in Commercial Distribution
• Version Model Number: 4420
• Catalog Number: 4420
• Company DUNS: 832696038
• Company Name: CAREFUSION 2200, INC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: false
• OTC Over-The-Counter: true

Customer Support Contacts

• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com
• Phone: +1(800)523-0502
• Email: Customer_Support@BD.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10885403142185 [Primary]
GS1	50885403142183 [Package]; Contains: 10885403142185; Package: Case [20 Units]; Discontinued: 2023-04-30; Not in Commercial Distribution

FDA Product Code

• OJU: Skin prep tray

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2024-02-23
• Device Publish Date: 2018-07-18

Devices Manufactured by CAREFUSION 2200, INC

• 10885403051722 - V. Mueller: 2024-05-03 LUMBAR AORTOGRAPHY NDL THINWALL 17GA 7IN
• 10885403049408 - V. Mueller: 2024-05-01 V. Mueller LEFORT URETHRAL SOUND 8FR, THREADED 1/56" FOR STD FILIFORM (NOT INCLUDED) OVERALL LENGTH 11" (28CM)
• 10885403071263 - V. Mueller: 2024-05-01 V. Mueller CHERRY S-SHAPED BRAIN RETRACTOR 10 AND 13MM WIDE OVERALL LENGTH 6-3/4" (17.1CM)
• 10885403105159 - V. Mueller: 2024-05-01 V. Mueller CRAIG TOOTHED CUTTER ONLY FOR CRAIG BIOPSY SET OVERALL LENGTH 7-3/8" (18.7CM)
• 20885403473170 - N/A: 2024-02-27 Surgical Clipper
• 50885403142176 - Wet Exidine: 2024-02-23 Wet Exidine-4 (CHG 4%) Preoperative Skin Prep Tray
• 50885403142183 - NA: 2024-02-23Wet PVP-I Small Procedure Preoperative Skin Prep Tray
• 50885403142183 - NA: 2024-02-23 Wet PVP-I Small Procedure Preoperative Skin Prep Tray
• 50885403142190 - NA: 2024-02-23 Dry Preoperative Skin Prep Tray With Powder-Free Gloves