FDA.reportPublic FDA data

HYBRID Guidewire

Primary DI
00818053022777
Brand
HYBRID Guidewire
Company
BALT USA LLC
Model
HYBRID007D.120
Device description
HYBRID Guidewire is a coiled wire that is designed to fit inside a percutaneous microcatheter for the purpose of directing the catheter through a blood vessel. It is used in association with catheters to enable insertion and easier navigation into the intracranial vascular branches for diagnositc or therapeutic use. Guidewires constitute an important element that conditions the success of the operation. They can be pushed and torqued to move forward through patient's tortuous anatomy.
Published
2018-12-01
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DQXWire, Guide, Catheter
MOFGuide, Wire, Catheter, Neurovasculature

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DQXWire, Guide, CatheterCardiovascular2
MOFGuide, Wire, Catheter, NeurovasculatureCardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K182337000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K182337000HYBRID GuidewireBalt USA, LLC2018-10-04MOF

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00818053022777PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00818053022777008180530227778180530227770818053022777

GMDN Terms#

Term, Definition table
TermDefinition
Cardiac/peripheral vascular guidewire, single-useA long, thin, sterile wire intended to be percutaneously placed into the cardiac vasculature (ventricles or coronary vessels) to function as a guide for the introduction, positioning, and/or operation of a device (e.g., catheter, pacing lead); it may also be used in the peripheral vasculature. It may be made of metal (e.g., stainless steel, Nitinol), or polymer and/or glass materials to provide MRI-compatibility, with or without coating, and is available in a variety of distal tip designs. It is used for various diagnostic and interventional procedures, and 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

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Special Storage Condition, Specify00Store in a dry place at room temperature and away from light

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
1-949-788-1443customerservice@balt-usa.com

Regulatory Flags#

DUNS number
945543689
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00840303713128Carrier XL Delivery CatheterCR8088142N/A2025-10-24
00840303713135Carrier XL Delivery CatheterCR8088162N/A2025-10-24
00840303713470Carrier XL Delivery CatheterCR8088152N/A2025-10-24
00840303713593Stellar Guide CatheterSTLR071125N/A2025-08-19
00840303713609Stellar Guide CatheterSTLR081105N/A2025-08-19
00840303713616Stellar Guide CatheterSTLR081115N/A2025-08-19
00840303713531Stellar Guide CatheterSTLR071105N/A2025-06-09
00840303713548Stellar Guide CatheterSTLR071110N/A2025-06-09
00840303713555Stellar Guide CatheterSTLR071115N/A2025-06-09
00840303713562Stellar Guide CatheterSTLR074105N/A2025-06-09
00840303713579Stellar Guide CatheterSTLR074110N/A2025-06-09
00840303713586Stellar Guide CatheterSTLR074115N/A2025-06-09
00840303713487Carrier™ Delivery CatheterCR7071162N/A2025-04-02
00840303713494Carrier™ Delivery CatheterCR7074162N/A2025-04-02
00840303713500Carrier™ Delivery CatheterCR8081162N/A2025-04-02
00840303711780MEGA Ballast Distal Access PlatformMEGABT09180N/A2025-02-19
00840303711797MEGA Ballast Distal Access PlatformMEGABT09190N/A2025-02-19
00840303711803MEGA Ballast Distal Access PlatformMEGABT091100N/A2025-02-19
00840303711810MEGA Ballast Distal Access PlatformMEGABT091110N/A2025-02-19
00840303711827MEGA Ballast Distal Access PlatformMEGABT09980N/A2025-02-19

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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00818075011261AristotleSCIENTIA VASCULAR LLCDQX2026-09-21
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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
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00884450739709InQwire®Merit Medical Systems, Inc.DQX2026-08-21
10801902226430ARROWTELEFLEX INCORPORATEDDQX2026-08-10
10801902206241ARROWTELEFLEX INCORPORATEDDQX2026-08-03
10801902192230ARROWTELEFLEX INCORPORATEDDQX2026-08-01
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10801902190908ARROWTELEFLEX INCORPORATEDDQX2026-07-30
10801902198461ARROWTELEFLEX INCORPORATEDDQX2026-07-30
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10705032057042AQUATRACK™ Hydrophilic Nitinol GuidewireCordis US Corp.DQX2026-07-29
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