Lifeport

FDA UDI

Class II (US FDA UDI)

by Navilyst Medical, Inc.

Identity

Trade Name: Lifeport FDA UDI
Generic Name: Vascular port/catheter FDA UDI
Device Name: Lifeport Single Plastic Port System with Attached 9.6F x 76cm Silicone Catheter FDA UDI
Model / Reference: LPS7015 FDA UDI
Description: Lifeport Single Plastic Port System with Attached 9.6F x 76cm Silicone Catheter FDA UDI

Identifiers

Primary DI / UDI-DI: H787LPS70150 FDA UDI
510(k) Number: K911355 FDA UDI
FDA Product Code: LJT FDA UDI
GMDN Term: Vascular port/catheter FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 880.5965 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

FDA UDI

MRI Safety

MR Conditional FDA UDI

Dimensions & Sizes

Size: Lumen/Inner Diameter — 1.5 Millimeter FDA UDI
Needle Gauge — 18 Gauge FDA UDI
Length — 76 Centimeter FDA UDI
Outer Diameter — 3.2 Millimeter FDA UDI
Catheter Gauge — 9.6 French FDA UDI

Category: Vascular port/catheter

Lifeport by Navilyst Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Navilyst Medical, Inc.

Sources (1)

FDA UDI bf2f4049-a7e1-448d-9714-4349db721329 36 fields · synced Jun 1, 2026