FDA UDI In Commercial Distribution 🇺🇸 United States

Lifeport

DI: H787LPS70150 · Model: LPS7015 · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
Lifeport
Primary DI
H787LPS70150
Version / Model
LPS7015
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
5
Public Version Date
2020-07-27
Public Version Status
Update
Public Device Record Key
bf2f4049-a7e1-448d-9714-4349db721329

Device Description

Lifeport Single Plastic Port System with Attached 9.6F x 76cm Silicone Catheter

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LJT PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR

GMDN Terms

Code Name
61494 Vascular port/catheter

Identifiers

Type ID
Primary H787LPS70150
Secondary 15051684018234

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K911355 000

Device Sizes

Type Value Unit Text
Lumen/Inner Diameter 1.5 Millimeter
Needle Gauge 18 Gauge
Length 76 Centimeter
Outer Diameter 3.2 Millimeter
Catheter Gauge 9.6 French