Centurion ART795

GUDID 00653160367683

ARTERIAL CATHETERIZATION KIT

CENTURION MEDICAL PRODUCTS CORPORATION

General surgical procedure kit, medicated

• Primary Device ID: 00653160367683
• NIH Device Record Key: a70f0ed1-a26d-49d9-8a37-8d3f046df69a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Centurion
• Version Model Number: ART795
• Catalog Number: ART795
• Company DUNS: 017246562
• Company Name: CENTURION MEDICAL PRODUCTS CORPORATION
• 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	00653160367683 [Package]; Contains: 10653160367680; Package: CASE [10 Units]; In Commercial Distribution
GS1	10653160367680 [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: 2023-11-13
• Device Publish Date: 2023-11-03

On-Brand Devices [Centurion]

• 10653160281542: LENSHOLDB20
• 10653160239000: MNS7300
• 10653160238997: IVS1350
• 10653160236030: CIT5100
• 10653160235460: CIT5095
• 10653160235354: CVI3335
• 10653160234227: CIT5075
• 10653160233954: IVS1200
• 10653160233442: PE2910
• 10653160233114: CIT5065
• 10653160233039: CIT5030
• 10653160233008: OR1821
• 10653160232230: CIT5045
• 10653160230748: MNS6940
• 10653160230670: CIT5010
• 10653160230601: HT5545
• 10653160230151: CIT5005
• 10653160229438: CIT5000
• 10653160229063: MNS6920
• 10653160228875: CIT4995
• 10653160228783: PE2900
• 10653160227366: CIT4980
• 10653160226147: CIT4915
• 10653160225133: OR1626
• 10653160224884: CIT4910
• 10653160224785: CIT4750
• 10653160224471: MNS6710
• 10653160223481: CIT4635
• 10653160222934: CIT4905
• 10653160222408: CIT4775
• 10653160222040: CIT4865
• 10653160222002: CIT4630
• 10653160221999: CIT4640
• 10653160221975: CIT4890
• 10653160221500: CIT4880
• 10653160221425: CIT4875
• 10653160221241: CIT4835
• 10653160221234: CIT4840
• 10653160220640: CIT4860
• 10653160219996: CIT4855
• 10653160219972: CIT4850
• 10653160218005: PE2875
• 10653160217916: CIT4800
• 10653160217404: CIT4795
• 10653160217381: PE2870
• 10653160216599: DT11955
• 10653160215714: CIT4770
• 10653160214922: MNS6395
• 10653160212553: MNS6330
• 10653160212362: CIT4691