STARTER™ GUIDE 49-121

GUDID 08714729743071

"J" Curved Fixed Core Guidewire

LAKE REGION MEDICAL LIMITED

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: 08714729743071
• NIH Device Record Key: 63a0c1ac-462a-49c6-a8b7-c48299f69527
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STARTER™ GUIDE
• Version Model Number: M001491211
• Catalog Number: 49-121
• Company DUNS: 988555595
• Company Name: LAKE REGION MEDICAL LIMITED
• 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

Customer Support Contacts

• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx
• Phone: 888-272-1001
• Email: xx@xx.xx

Device Dimensions

• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter
• Outer Diameter: 0.035 Inch
• Length: 260 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729326540 [Primary]
GS1	08714729743071 [Package]; Contains: 08714729326540; 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: 2016-11-06

Devices Manufactured by LAKE REGION MEDICAL LIMITED

• 08714729743156 - Starter™ Guidewire: 2021-12-22 "J" Curved Moveable Core Guidewire
• 08714729201281 - Starter™ Guidewire: 2021-12-22 Straight Fixed Core Guidewire
• 08714729742999 - Starter™ Guidewire: 2021-12-22 Straight Moveable Core Guidewire
• 08714729743040 - Starter™ Guidewire: 2021-12-22 "J" Curved Fixed Core Guidewire
• 08714729743125 - Starter™ Guidewire: 2021-12-22 "J" Curved Moveable Core Guidewire
• 08714729743200 - Starter™ Guidewire: 2021-12-22 Bentson Guidewire
• 08714729742951 - Starter™ Guidewire: 2021-12-22 Straight Fixed Core Guidewire
• 08714729326465 - Starter™ Guidewire: 2021-12-22 Straight Fixed Core Guidewire