Lifeport

GUDID H787LPS75230

Lifeport Dual Plastic Port System with Attachable 9.6F x 76cm Polyurethane Catheter

NAVILYST MEDICAL, INC.

Infusion/injection port, implantable

• Primary Device ID: H787LPS75230
• NIH Device Record Key: fa72abe9-fa75-4879-8a7b-4cc6e4ced83a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lifeport
• Version Model Number: LPS7523
• Company DUNS: 809699023
• Company Name: NAVILYST MEDICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: true
• 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(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com
• Phone: +1(518)795-1676
• Email: dgreer@angiodynamics.com

Device Dimensions

• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter
• Catheter Gauge: 9.6 French
• Outer Diameter: 3.2 Millimeter
• Length: 76 Centimeter
• Needle Gauge: 18 Gauge
• Lumen/Inner Diameter: 1.4 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	H787LPS75230 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K905849

FDA Product Code

• LJT: PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

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: 2018-07-06
• Device Publish Date: 2018-02-07

On-Brand Devices [Lifeport ]

• H787LPS30255: LifePort Infusion Set
• H787LPS30235: LifePort Infusion Set
• H787LPS30175: LifePort Infusion Set
• H787LPS30095: LifePort Infusion Set
• H787LPS30085: LifePort Infusion Set
• H787LPS30075: LifePort Infusion Set
• H787LPS30065: LifePort Infusion Set
• H787LPS30055: LifePort Infusion Set
• H787LPS30045: LifePort Infusion Set
• H787LPS70150: Lifeport Single Plastic Port System with Attached 9.6F x 76cm Silicone Catheter
• H787LPS70130: Lifeport Single Plastic Port System with Attachable 9.6F x 76cm Silicone Catheter
• H787LPS50570: Lifeport Low Profile Titanium Port System with Detached 8.4F/9.6F x 76cm Silicone Catheter
• H787LPS50130: Lifeport Single Titanium Port System with Attachable 9.6F x 76cm Silicone Catheter
• H787LPS75230: Lifeport Dual Plastic Port System with Attachable 9.6F x 76cm Polyurethane Catheter
• H787LPS75130: Lifeport Single Plastic Port System with Attachable 8.4F x 76cm Polyurethane Catheter
• H787LPS72550: Lifeport Dual Low Profile Plastic Port System with Attachable Dual Lumen 6.6F x 76cm Polyurethan
• H787LPS55130: Lifeport Single Titanium Port System with Attachable 8.4F x 76cm Polyurethane Catheter