Bendit2.7 Steerable Microcatheter

GUDID 17290018072001

The Bendit2.7™ Steerable Microcatheter is intended for general intravascular use in the peripheral vasculature. The microcatheter can be used for the delivery of diagnostic, embolic, or therapeutic materials into the vasculature.

BEND IT TECHNOLOGIES LTD

Vascular microcatheter

• Primary Device ID: 17290018072001
• NIH Device Record Key: b1b6d21d-e948-46c0-9e97-d6217d549e5e
• Commercial Distribution Discontinuation: 2050-08-24
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bendit2.7 Steerable Microcatheter
• Version Model Number: BDT01200
• Company DUNS: 600476669
• Company Name: BEND IT TECHNOLOGIES LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• 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: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com
• Phone: +97236747377
• Email: info@bendittech.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	17290018072001 [Primary]
GS1	27290018072008 [Package]; Package: [1 Units]; Discontinued: 2030-12-31; In Commercial Distribution
GS1	37290018072005 [Package]; Contains: 27290018072008; Package: [3 Units]; Discontinued: 2030-12-31; In Commercial Distribution
GS1	47290018072002 [Package]; Contains: 27290018072008; Package: [5 Units]; Discontinued: 2030-12-31; In Commercial Distribution
GS1	57290018072009 [Package]; Contains: 27290018072008; Package: [10 Units]; Discontinued: 2030-12-31; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K200582

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: 2020-09-01
• Device Publish Date: 2020-08-24

Devices Manufactured by BEND IT TECHNOLOGIES LTD

• 17290018072049 - Bendit®21 Microcatheter: 2022-06-17 The Bendit®21 Microcatheter is intended for use in accessing target locations in the peripheral, coronary, and neuro vasculatur
• 17290018072001 - Bendit2.7 Steerable Microcatheter: 2020-09-01The Bendit2.7™ Steerable Microcatheter is intended for general intravascular use in the peripheral vasculature. The microcatheter can be used for the delivery of diagnostic, embolic, or therapeutic materials into the vasculature.
• 17290018072001 - Bendit2.7 Steerable Microcatheter: 2020-09-01 The Bendit2.7™ Steerable Microcatheter is intended for general intravascular use in the peripheral vasculature. The microcathe