Primary Device ID | 00884521060824 |
NIH Device Record Key | bf9297f6-c690-457d-8522-cd04f94ff719 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Argyle |
Version Model Number | 8888570515 |
Catalog Number | 8888570515 |
Company DUNS | 080935429 |
Company Name | Cardinal Health, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | true |
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(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com | |
Phone | +1(508)261-8000 |
covidien.udi@covidien.com |
Catheter Gauge | 16 French |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Length | 50 Centimeter |
Catheter Gauge | 16 French |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Special Storage Condition, Specify | Between 0 and 0 *Keep dry;AVOID DIRECT SUNLIGHT |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884521060824 [Package] Contains: 00884521149413 Package: CASE [10 Units] In Commercial Distribution |
GS1 | 00884521149413 [Primary] |
JOL | CATHETER AND TIP, SUCTION |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2019-02-15 |
Device Publish Date | 2017-05-10 |
00884521074067 | Flexible Yankauer,Large Tip, No Vacuum Control |
20884521101774 | Poole Suction Instrument,Rigid |
00884521139360 | Aortic Perfusion Cannula,Angled Tip |
00884521139377 | Aortic Perfusion Cannula,Angled Tip |
00884521139384 | Aortic Perfusion Cannula,Straight Tip |
00884521139391 | Aortic Perfusion Cannula,Straight Tip |
00884521139353 | Aortic Perfusion Cannula,Angled Tip |
00884521063238 | Aortic Perfusion Cannula,Angled Tip |
00884521063221 | Aortic Perfusion Cannula,Angled Tip |
00884521063214 | Aortic Perfusion Cannula,Angled Tip |
00884521060886 | Thoracic Catheter,Straight |
00884521060879 | Thoracic Catheter,Straight |
00884521060862 | Thoracic Catheter,Straight |
00884521060855 | Thoracic Catheter,Straight |
00884521060848 | Thoracic Catheter,Straight |
00884521060831 | Thoracic Catheter,Straight |
00884521060824 | Thoracic Catheter,Straight |
00884521060817 | Thoracic Catheter,Straight |
00884521149277 | Penrose Tubing Radiopaque |
00884521067533 | Penrose Tubing Radiopaque |
00884521067526 | Penrose Tubing Radiopaque |
20884521067513 | Penrose Tubing Radiopaque |
00884521067496 | Penrose Tubing Radiopaque |
00884521067489 | Penrose Tubing Radiopaque |
00884521067472 | Penrose Tubing Radiopaque |
00884521149147 | Penrose Tubing Radiopaque |
20884521067452 | Penrose Tubing Radiopaque |
00884521149123 | Penrose Tubing Radiopaque |
20884521067438 | Penrose Tubing Radiopaque |
10884521067424 | Penrose Tubing Radiopaque |
00884521071356 | Penrose Tubing Radiopaque |
00884521067403 | Penrose Tubing Radiopaque |
00884521073312 | Gentle Flow Suction Catheter,Vacuum Control |
00884521142001 | Left Ventricular Catheter,Ferguson, Radiopaque Line and Eye |
00884521061036 | Carotid Artery Shunt Kit,Radiopaque Line, Straight |
00884521088187 | Female Luer Adapter |
00884521115913 | One Bottle Drainage System,9/32 inch (0.7 cm) Tubing |
00884521074074 | Flexible Yankauer,Fine Tip, No Vacuum Control |
00884521074050 | Flexible Yankauer,Medium Sump Tip, Vacuum Control |
00884521074029 | Flexible Yankauer,Medium Tip, No Vacuum Control |
00884521061043 | Vascular Tourniquet Kit |
00884521071899 | Saratoga Sump Drain |
00884521071882 | Saratoga Sump Drain |
00884521071875 | Saratoga Sump Drain |
20884527001863 | Graduated Suction Catheter Tray with Chimney Valve,Sterile Water |
10884521002999 | Surgical Aspirator Tip,Regular Opening, Opaque |
10884527020041 | Hydrogel Adhesive Baby Tape Strips |
20884527004635 | Infant Heel Warmer,Attachment Tab |
20884527004628 | Infant Heel Warmer,No Attachment Tab |
10884527000197 | Suction Catheter with Mucus Trap,20 mL |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() ARGYLE 98315933 not registered Live/Pending |
Argyle Build Inc. 2023-12-15 |
![]() ARGYLE 98235599 not registered Live/Pending |
Argyle Systems Inc. 2023-10-23 |
![]() ARGYLE 97505323 not registered Live/Pending |
Toledo Spirits Company, LLC 2022-07-15 |
![]() ARGYLE 90298832 not registered Live/Pending |
ARGYLE SYSTEMS INC. 2020-11-04 |
![]() ARGYLE 88847562 not registered Live/Pending |
Footwear Industries Pty Ltd 2020-03-25 |
![]() ARGYLE 87277027 not registered Live/Pending |
Argyle Diamonds Limited 2016-12-21 |
![]() ARGYLE 87038638 5915156 Live/Registered |
UPL NA INC. 2016-05-16 |
![]() ARGYLE 86091179 5311555 Live/Registered |
Argyle Data, Inc. 2013-10-14 |
![]() ARGYLE 85704405 4495604 Live/Registered |
Omarzai, Reza 2012-08-15 |
![]() ARGYLE 77726531 not registered Dead/Abandoned |
Callaway Golf Company 2009-04-30 |
![]() ARGYLE 77085765 not registered Dead/Abandoned |
Winter, Michael 2007-01-18 |
![]() ARGYLE 77084822 not registered Dead/Abandoned |
GAV LLC 2007-01-17 |