INPUT™ PS

GUDID 20643169014101

INTRDCR 090023 5PK 9F 23CM INPT INTR KIT

MEDTRONIC, INC.

Vascular catheter introduction set, nonimplantable

• Primary Device ID: 20643169014101
• NIH Device Record Key: 03f046c6-9d18-4b6f-a805-1557ebc17c85
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: INPUT™ PS
• Version Model Number: 090023
• Company DUNS: 006261481
• Company Name: MEDTRONIC, 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: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

• Length: 23 Centimeter
• Length: 23 Centimeter
• Length: 23 Centimeter
• Length: 23 Centimeter
• Length: 23 Centimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter
• Catheter Gauge: 9 French
• Outer Diameter: 0.97 Millimeter
• Length: 23 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00643169014107 [Primary]
GS1	20643169014101 [Package]; Contains: 00643169014107; Package: PK [5 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132617

FDA Product Code

• DYB: INTRODUCER, CATHETER

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: 2019-06-07
• Device Publish Date: 2017-02-02

On-Brand Devices [INPUT™ PS]

• 20643169014651: INTRDCR 060011 5PK 6F 11CM INPT INTR KIT
• 20643169014644: INTRDCR 060023 5PK 6F 23CM INPT INTR KIT
• 20643169014583: INTRDCR 070011 5PK 7F 11CM INPT INTR KIT
• 20643169014576: INTRDCR 070023 5PK 7F 23CM INPT INTR KIT
• 20643169014514: INTRDCR 080011 5PK 8F 11CM INPT INTR KIT
• 20643169014507: INTRDCR 080023 5PK 8F 23CM INPT INTR KIT
• 20643169014330: INTRDCR 050011 5PK 5F 11CM INPT INTR KIT
• 20643169014293: INTRDCR 090011 5PK 9F 11CM INPT INTR KIT
• 20643169014279: INTRDCR 553311 5F 5PK 5F 11CM INPUT
• 20643169014262: INTRDCR 563311 6F 5PK 6F 11CM INPUT
• 20643169014255: INTRDCR 573311 7F 5PK 7F 11CM INPUT
• 20643169014248: INTRDCR 583311 8F 5PK 8F 11CM INPUT
• 20643169014231: INTRDCR 593311 9F 5PK 9F 11CM INPUT
• 20643169014163: INTRDCR 853311 5F 5PK 5F 11CM INPUT
• 20643169014156: INTRDCR 863311 6F 5PK 6F 11CM INPUT
• 20643169014149: INTRDCR 873311 7F 5PK 7F 11CM INPUT
• 20643169014132: INTRDCR 883311 8F 5PK 8F 11CM INPUT
• 20643169014125: INTRDCR 893311 9F 5PK 9F 11CM INPUT
• 20643169014101: INTRDCR 090023 5PK 9F 23CM INPT INTR KIT