FDA.reportPublic FDA data

Shepherd

Primary DI
30850026568654
Brand
Shepherd
Company
Cardiovascular Systems, Inc.
Model
PSP14S-19530
Catalog number
7-10097-05
Device description
0.014" Shepherd ES Guidewire - straight 195 cm - 30 gms
Published
2022-05-20
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQXWire, Guide, Catheter

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQXWire, Guide, CatheterCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
30850026568654PackageGS15In Commercial Distribution
10850026568650PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
3085002656865430850026568654
1085002656865010850026568650

GMDN Terms#

Term, Definition table
TermDefinition
Peripheral vascular guidewire, manualA long, thin wire intended to be percutaneously placed into the peripheral vasculature (not heart or central nervous system) to function as a guide for the introduction of devices (e.g., catheters). It is made of metal (e.g., stainless steel, Nitinol), with or without coating, and is available in a variety of distal tip designs. It is intended to be used for percutaneous angiography, angioplasty, rotational atherectomy and thrombectomy, drainage, and other diagnostic and interventional procedures. It may include devices used to facilitate manipulation (e.g., torque device). This is a single-use device.

Device Sizes#

Type, Value, Unit table
TypeValueUnit
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Guidewire Diameter0.014Inch
Length195Centimeter

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
651-259-1600customerservice@csi360.com

Regulatory Flags#

DUNS number
024954518
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
10852528005688ViperCath XC035-XC-200-07-10043-012019-02-04
10852528005695ViperCath XC035-XC-200-17-10043-022019-02-04
10852528005817Diamondback PeripheralDBP-EX-125MIC1457-10030-012019-02-04
10852528005824Diamondback PeripheralDBP-EX-125SOL1457-10030-022019-02-04
10852528005831Diamondback PeripheralDBP-EX-150SOL1457-10030-032019-02-04
10852528005848Diamondback PeripheralDBP-EX-200SOL1457-10030-042019-02-04
10852528005862Diamondback PeripheralDBP-EX-125SOL757-10030-062019-02-04
10852528005879Diamondback PeripheralDBP-EX-125SOL2007-10030-072019-02-04
10852528005886Diamondback PeripheralDBP-EX-150SOL2007-10030-082019-02-04
10852528005893Diamondback PeripheralDBP-EX-175SOL1807-10030-092019-02-04
10852528005909Diamondback PeripheralDBP-EX-150CLA1457-10030-102019-02-04
10852528005916Diamondback PeripheralDBP-EX-200CLA1457-10030-112019-02-04
10852528005855Diamondback PeripheralDBP-EX-125MIC757-10030-052019-02-04
10850000491172Diamondback PeripheralDBP-125MICRO1457-10057-012019-11-13
10850000491189Diamondback PeripheralDBP-125SOLID1457-10057-022019-11-13
10850000491196Diamondback PeripheralDBP-150SOLID1457-10057-032019-11-13
10850000491202Diamondback PeripheralDBP-200SOLID1457-10057-042019-11-13
10850000491219Diamondback PeripheralDBP-125SOLID2007-10057-052019-11-13
10850000491226Diamondback PeripheralDBP-150SOLID2007-10057-062019-11-13
10850000491233Diamondback PeripheralDBP-175SOLID1807-10057-072019-11-13

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00818075011261AristotleSCIENTIA VASCULAR LLCDQX2026-09-21
10801902226614ARROWTELEFLEX INCORPORATEDDQX2026-08-28
00884450529300SplashWire™Merit Medical Systems, Inc.DQX2026-08-21
00884450529713SplashWire™Merit Medical Systems, Inc.DQX2026-08-21
00884450529829SplashWire™Merit Medical Systems, Inc.DQX2026-08-21
00884450590010SplashWire™Merit Medical Systems, Inc.DQX2026-08-21
00884450631928InQwire® AmplatzMerit Medical Systems, Inc.DQX2026-08-21
00884450731789InQwire®Merit Medical Systems, Inc.DQX2026-08-21
00884450739709InQwire®Merit Medical Systems, Inc.DQX2026-08-21
10801902226430ARROWTELEFLEX INCORPORATEDDQX2026-08-10
10801902206241ARROWTELEFLEX INCORPORATEDDQX2026-08-03
10801902192230ARROWTELEFLEX INCORPORATEDDQX2026-08-01
04547327167215CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
04547327167222CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
04547327167239CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
04547327167246CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
04547327167253CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
04547327167260CROSSLOOPASAHI INTECC CO., LTD.DQX2026-07-31
10801902190908ARROWTELEFLEX INCORPORATEDDQX2026-07-30
10801902198461ARROWTELEFLEX INCORPORATEDDQX2026-07-30
10705032057004AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057011AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057028AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057035AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057042AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057059AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057066AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057073AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10705032057080AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
10801902193237ARROWTELEFLEX INCORPORATEDDQX2026-07-29