Rebar

GUDID 00763000412487

MICRO CATH 105-5081-153 V05 REBAR

Micro Therapeutics, Inc.

Vascular microcatheter

• Primary Device ID: 00763000412487
• NIH Device Record Key: bf8a4444-c703-4bb4-8a30-5d7093347847
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Rebar
• Version Model Number: 105-5081-153
• Company DUNS: 826110710
• Company Name: Micro Therapeutics, Inc.
• 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: false
• Expiration Date: false
• 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: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Operating and Storage Conditions

• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight
• Special Storage Condition, Specify: Between 0 and 0 *Device should be stored in a dry place, away from sunlight

Device Identifiers

Device Issuing Agency	Device ID
GS1	00763000412487 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K093750

FDA Product Code

• KRA: Catheter, continuous flush

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-08-16
• Device Publish Date: 2024-08-08

On-Brand Devices [Rebar]

• 00836462002135: 105-5080-153 REBAR-14 153CM
• 00836462002234: 18 Micro Catheter
• 00836462002227: 027 Micro Catheter
• 00836462002210: MICRO CATH 105-5082-130 REBAR IR
• 00836462002197: MICRO CATH 105-5081-153 REBAR IR
• 00836462002180: 18 Micro Catheter
• 00836462002142: 14 Micro Catheter
• 00836462002081: 105-5078-153 REBAR10 153CM MICRO CATH
• 00763000539375: MICRO CATHETER 105-5083-153 V08
• 00763000539368: MICRO CATHETER 105-5082-145 V08
• 00763000539351: MICRO CATHETER 105-5082-130 V08
• 00763000539344: MICRO CATHETER 105-5081-153 V08 SMB
• 00763000539337: MICRO CATHETER 105-5081-130 V08
• 00763000412487: MICRO CATH 105-5081-153 V05 REBAR