Primary Device ID | 15051684018753 |
NIH Device Record Key | 294cbb59-60f4-4703-b015-3113b95652fc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BioFlo |
Version Model Number | 44023 |
Company DUNS | 079252781 |
Company Name | Angiodynamics, 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 |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com | |
Phone | +1(800)772-6446 |
customerservice@angiodynamics.com |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Lumen/Inner Diameter | 1.3 Millimeter |
Length | 63 Centimeter |
Catheter Gauge | 6 French |
Outer Diameter | 2.1 Millimeter |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15051684018753 [Primary] |
HIBCC | H965440230 [Previous] |
LJT | PORT & CATHETER, IMPLANTED, SUBCUTANEOUS, INTRAVASCULAR |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-09-30 |
Device Publish Date | 2024-09-20 |
15051684018784 | BioFlo Dual Port with Endexo Technology - Plastic Port with Filled Suture Holes and 8F Polyureth |
15051684018777 | BioFlo Dual Port with Endexo Technology - Plastic Port with Non-Filled Suture Holes and 8F Polyu |
15051684018753 | BioFlo Titanium Port with PASV Valve Technology (Non-Filled Suture Holes) and 6F x 63cm Polyure |
15051684018746 | BioFlo Plastic Port with PASV Valve Technology (Filled Suture Holes) and 8F x 63cm Polyurethane |
15051684018708 | BioFlo Titanium Port with Non Filled Suture Holes and 8F x 63cm Polyurethane Catheter with ENDEX |
15051684018692 | BioFlo Titanium Port with Non Filled Suture Holes and 6F x 63cm Polyurethane Catheter with ENDEX |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BIOFLO 98572768 not registered Live/Pending |
FloSpine 2024-05-28 |
BIOFLO 98490320 not registered Live/Pending |
Allegheny Petroleum Products Company 2024-04-09 |
BIOFLO 90038587 not registered Live/Pending |
Industrial Systems 2020-07-07 |
BIOFLO 87649723 5485529 Live/Registered |
AngioDynamics, Inc. 2017-10-18 |
BIOFLO 86893560 5103418 Live/Registered |
AngioDynamics, Inc. 2016-02-01 |
BIOFLO 86729361 not registered Dead/Abandoned |
AngioDynamics, Inc. 2015-08-19 |
BIOFLO 86423436 4751648 Live/Registered |
AngioDynamics, Inc. 2014-10-14 |
BIOFLO 85564026 4362153 Live/Registered |
Bioflo, Inc. 2012-03-08 |
BIOFLO 85179751 4350554 Live/Registered |
BIOFLO LLC 2010-11-18 |
BIOFLO 76497412 2977255 Dead/Cancelled |
HYDOR S.R.L. 2003-03-14 |
BIOFLO 76469903 2779330 Live/Registered |
EPPENDORF, INC. 2002-11-25 |
BIOFLO 76209114 2687961 Live/Registered |
Allegheny Bradford Corporation 2001-02-12 |