Jetstream™ Jetwire

GUDID 08714729888789

Lake Region Medical

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 ID: 08714729888789
• NIH Device Record Key: 730afc9a-524b-4338-8ec2-d554d010b5d4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Jetstream™ Jetwire
• Version Model Number: 011525-000
• Company DUNS: 031108704
• Company Name: Lake Region Medical
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter
• Outer Diameter: 0.014 Inch
• Length: 300 Centimeter

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.
• Special Storage Condition, Specify: Between 0 and 0 *Keep dry. Keep away from sunlight. Store in a cool, dry place.

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729888772 [Primary]
GS1	08714729888789 [Package]; Contains: 08714729888772; Package: [5 Units]; In Commercial Distribution

FDA Product Code

• DQX: Wire, Guide, Catheter

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2021-12-22
• Device Publish Date: 2016-10-31

Devices Manufactured by Lake Region Medical

• 08714729839873 - NaviPro™: 2023-12-06
• 8714729839866 - NaviPro™: 2023-12-06
• 08714729839897 - NaviPro™: 2023-12-06
• 08714729839880 - NaviPro™: 2023-12-06
• 08714729839910 - NaviPro™: 2023-12-06
• 08714729839903 - NaviPro™: 2023-12-06
• 08714729839934 - NaviPro™: 2023-12-06
• 08714729839927 - NaviPro™: 2023-12-06