OTHER RW-1023CT

GUDID 00653160365542

DRESSING CHANGE TRAY

MEDLINE INDUSTRIES, INC.

General surgical procedure kit, medicated

• Primary Device ID: 00653160365542
• NIH Device Record Key: 90f7958c-281b-4f1c-ae18-fda165018636
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OTHER
• Version Model Number: RW-1023CT
• Catalog Number: RW-1023CT
• Company DUNS: 025460908
• Company Name: MEDLINE INDUSTRIES, INC.
• Device Count: 1
• DM Exempt: true
• 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: true
• 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)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM
• Phone: +1(800)633-5463
• Email: CUSTOMERSERVICE@MEDLINE.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00653160365542 [Package]; Contains: 10653160365549; Package: CASE [30 Units]; In Commercial Distribution
GS1	10653160365549 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K213481

FDA Product Code

• LRO: General surgery tray

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-13
• Device Publish Date: 2023-09-05

On-Brand Devices [OTHER]

• 20193489111191: DRESSING CHANG W/PREVANTICS SWABS
• 20193489111207: DRESSING CHANG W/PVP SWABSTICKS
• 20193489111214: IV START KIT
• 40860000300634: TREATMENT PACK
• 00653160323795: ARTERIAL LINE START KIT W/O CATH
• 40889942266839: ARTHROGRAM PACK
• 00653160328936: CIRCUMCISION TRAY
• 00653160278293: HUBGUARD FM TP STRPS (MED ALLIANCE ONLY)
• 00653160267211: DAILY DRIVELINE DRESSING SYSTEM
• 10653160193944: HUBGUARD CATHETER SECUREMENT STRIPS
• 10653160113300: NEONATAL COMPONENT TRAY T70-012-07
• 00653160353754: DRESSING CHANGE
• 00653160355772: DRESSING CHANGE TRAY
• 00653160362183: RWM DRESSING CHANGE TRAY, CHLORAPREP, ON
• 00653160365542: DRESSING CHANGE TRAY
• 00653160364767: ARTERIAL LINE START KIT W/O CATH
• 00653160370836: DRESSING CHANGE TRAY
• 00653160370270: RWM DRESSING CHANGE TRAY, CHLORHEXIDINE
• 00653160374957: KIT INFLATION DEVICE 125 Y ADAPTER
• 00653160374131: BONE MARROW KIT
• 10653160374992: KIT INFLATION DEVICE LB Y ADAPTER
• 10653160374985: KIT INFLATION DEVICE GTWY Y ADAPTER
• 20197344110794: KIT INFLATION DEVICE DIGITAL