CLEARWAY

GUDID 00650862802207

CLEARWAY, RX 2.50X20MM

ATRIUM MEDICAL CORPORATION

Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter Peripheral vascular intervention infusion catheter
Primary Device ID00650862802207
NIH Device Record Key026bc18c-e2ab-498e-baaa-613822c7f0a9
Commercial Distribution StatusIn Commercial Distribution
Brand NameCLEARWAY
Version Model Number80220
Company DUNS051798999
Company NameATRIUM MEDICAL CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100650862802207 [Primary]

FDA Product Code

DQYCATHETER, PERCUTANEOUS

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2019-04-09
Device Publish Date2015-09-24

On-Brand Devices [CLEARWAY]

00650862802535CLEARWAY, RX 4.00X50MM
00650862802504CLEARWAY, RX 4.00X20MM
00650862802443CLEARWAY, RX 3.50X20MM
00650862802351CLEARWAY, RX 3.00X50MM
00650862802320CLEARWAY, RX 3.00X20MM
00650862802207CLEARWAY, RX 2.50X20MM
00650862802177CLEARWAY, RX 2.00X50MM
00650862802146CLEARWAY, RX 2.00X20MM
00650862802085CLEARWAY, RX 1.50X20MM
00650862802023CLEARWAY, RX 1.00X20MM
00650862802009CLEARWAY, RX 1.00X10MM

Trademark Results [CLEARWAY]

Mark Image

Registration | Serial
Company
Trademark
Application Date
CLEARWAY
CLEARWAY
97710556 not registered Live/Pending
1345750 B.C. Ltd.
2022-12-09
CLEARWAY
CLEARWAY
97423751 not registered Live/Pending
Secrets of the Tribe
2022-05-23
CLEARWAY
CLEARWAY
90664503 not registered Live/Pending
Electromed, Inc.
2021-04-22
CLEARWAY
CLEARWAY
88296270 not registered Live/Pending
ANSwers Neuroscience, Inc.
2019-02-11
CLEARWAY
CLEARWAY
88266227 not registered Live/Pending
ANSwers Neuroscience, Inc.
2019-01-17
CLEARWAY
CLEARWAY
88101258 not registered Live/Pending
Zephyr Renewables LLC
2018-08-31
CLEARWAY
CLEARWAY
87831994 5729489 Live/Registered
Clearway Pain Solutions Institute, LLC
2018-03-13
CLEARWAY
CLEARWAY
87021600 5498368 Live/Registered
Eastman Chemical Company
2016-05-02
CLEARWAY
CLEARWAY
86117832 4739990 Live/Registered
TracFone Wireless, Inc.
2013-11-13
CLEARWAY
CLEARWAY
79251619 5929357 Live/Registered
EXTRUFLEX
2018-11-12
CLEARWAY
CLEARWAY
79096792 4262886 Live/Registered
EXTRUFLEX
2011-03-31
CLEARWAY
CLEARWAY
78847558 3473886 Live/Registered
CLEARWAY MINNESOTA
2006-03-28

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.