FDA UDI Not in Commercial Distribution 🇺🇸 United States

Vortex

DI: H787P12305K0 · Model: P12305K · ANGIODYNAMICS, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vortex
Primary DI
H787P12305K0
Version / Model
P12305K
Company Name
ANGIODYNAMICS, INC.
Labeler DUNS
601994184
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
4
Public Version Date
2021-11-30
Public Version Status
Update
Public Device Record Key
a9fb897d-57cd-4385-b626-aa23936e6ffc
Distribution End Date
2021-11-23

Device Description

Vortex LP Single Titanium Port System with Attachable 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 H787P12305K0

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K010189 000

Device Sizes

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