DIAMONDBACK 7-10057-10

GUDID 10850026568445

DIAMONDBACK PERIPHERAL, MAX CROWN, 2.00MM, 145CM SHAFT

Cardiovascular Systems, Inc.

Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral Mechanical atherectomy system catheter, peripheral
Primary Device ID10850026568445
NIH Device Record Key00d865e5-1433-49bd-ab3d-525cf5449eb1
Commercial Distribution StatusIn Commercial Distribution
Brand NameDIAMONDBACK
Version Model NumberDBP-200MAX145
Catalog Number7-10057-10
Company DUNS024954518
Company NameCardiovascular Systems, Inc.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com
Phone651-259-1600
Emailcustomerservice@csi360.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110850026568445 [Primary]

FDA Product Code

MCWCatheter, Peripheral, Atherectomy

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-07-11
Device Publish Date2022-07-01

On-Brand Devices [DIAMONDBACK]

10850026568476DIAMONDBACK EXCHANGEABLE SYSTEM, 2.00 MAX CROWN, 145CM SHAFT
10850026568469DIAMONDBACK EXCHANGEABLE CARTRIDGE, 2.00 MAX CROWN, 145CM SHAFT
10850026568445DIAMONDBACK PERIPHERAL, MAX CROWN, 2.00MM, 145CM SHAFT

Trademark Results [DIAMONDBACK]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DIAMONDBACK
DIAMONDBACK
97529434 not registered Live/Pending
Texxstar Resources (USA), Inc.
2022-08-01
DIAMONDBACK
DIAMONDBACK
97502872 not registered Live/Pending
CrawlSpaceRepair.com, LLC
2022-07-14
DIAMONDBACK
DIAMONDBACK
97174148 not registered Live/Pending
US SYNTHETIC CORPORATION
2021-12-15
DIAMONDBACK
DIAMONDBACK
97171800 not registered Live/Pending
Alta Cycling Group IP Holder, LLC
2021-12-14
DIAMONDBACK
DIAMONDBACK
88936169 not registered Live/Pending
Big Lake Tackle Company
2020-05-27
DIAMONDBACK
DIAMONDBACK
88468240 not registered Live/Pending
Sheltered Wings, Inc.
2019-06-11
DIAMONDBACK
DIAMONDBACK
88465944 not registered Live/Pending
Diamondback Tool Co. Inc.
2019-06-10
DIAMONDBACK
DIAMONDBACK
88367576 not registered Live/Pending
Fluid Handling LLC
2019-04-02
DIAMONDBACK
DIAMONDBACK
87868073 5611341 Live/Registered
Epiroc Drilling Solutions LLC
2018-04-09
DIAMONDBACK
DIAMONDBACK
87809977 5575322 Live/Registered
Diamondback International, Inc.
2018-02-25
DIAMONDBACK
DIAMONDBACK
87524627 not registered Dead/Abandoned
Crosman Corporation
2017-07-12
DIAMONDBACK
DIAMONDBACK
87273168 5255291 Live/Registered
Mitsubishi Electric US, Inc.
2016-12-19

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