FDA UDI In Commercial Distribution 🇺🇸 United States

Vortex

DI: H787MPP5PT0 · Model: MP-P5PT · NAVILYST MEDICAL, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

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Basic Information

Brand Name
Vortex
Primary DI
H787MPP5PT0
Version / Model
MP-P5PT
Company Name
NAVILYST MEDICAL, INC.
Labeler DUNS
809699023
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-02-07
Public Version
5
Public Version Date
2020-07-27
Public Version Status
Update
Public Device Record Key
4f740040-9323-4af4-8333-5a9ea3ed7297

Device Description

Vortex MP Low Profile Titanium Port System with Attachable 5F x 76cm Polyurethane 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 H787MPP5PT0
Secondary 15051684018340

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K033473 000

Device Sizes

Type Value Unit Text
Needle Gauge 18 Gauge
Lumen/Inner Diameter 1 Millimeter
Outer Diameter 1.7 Millimeter
Catheter Gauge 5 French
Length 76 Centimeter