ViperWire VPR-GW-200

GUDID 30852528005224

VIPERWIRE, ADVANCED, .012" DIA .012" SPRING TIP, 200CM, 5 PACK

Cardiovascular Systems, Inc.

Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual Peripheral vascular guidewire, manual
Primary Device ID30852528005224
NIH Device Record Key782c56b9-bb26-4a5f-a48c-4fc828810b0c
Commercial Distribution StatusIn Commercial Distribution
Brand NameViperWire
Version Model NumberVPR-GW-200
Catalog NumberVPR-GW-200
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
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

Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0
Length200 Centimeter
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110852528005220 [Primary]
GS130852528005224 [Package]
Contains: 10852528005220
Package: Box [5 Units]
In Commercial Distribution

FDA Product Code

MCWCatheter, Peripheral, Atherectomy

Sterilization

Steralize Prior To Usetrue
Device Is Steriletrue

[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


[30852528005224]

Ethylene Oxide


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2021-12-22
Device Publish Date2015-12-04

Devices Manufactured by Cardiovascular Systems, Inc.

10852528005169 - Diamondback Coronary2023-12-18 DIAMONDBACK CORONARY, CLASSIC CROWN, 1.25MM
10852528005176 - Diamondback Coronary2023-12-18 CORONARY ELECTRIC, CLASSIC CROWN, 1.50MM
30852528005187 - Diamondback Coronary2023-12-18 Guidewire, Viperwire Adavnce Coronary Floppy, .012: dia, .014" Spring Tip, 1 Pack 325 cm
10852528005336 - Diamondback Coronary2023-12-18 DIAMONDBACK 360® Coronary Orbital Atherectomy System, Micro Crown
10852528005428 - Diamondback Coroanry2023-12-18 CORONARY ELECTRIC, CLASSIC CROWN, 1.25MM
10852528005787 - Diamondback Coronary2023-12-18 CORONARY ELECTRIC, CLASSIC CROWN, 1.25MM
10852528005800 - Diamondback Coronary2023-12-18 SALINE INFUSION PUMP (SIP)
10852528005442 - Diamondback Coronary2023-12-11 SALINE INFUSION PUMP (SIP)

Trademark Results [ViperWire]

Mark Image

Registration | Serial
Company
Trademark
Application Date
VIPERWIRE
VIPERWIRE
77210006 3644144 Live/Registered
Cardiovascular Systems, Inc.
2007-06-19

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