iTind Removal Kit

GUDID 07290015518192

iTind Removal Kit: 1 Snare + 1 Removal Tube

MEDI-TATE LTD

Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term Bare-metal urethral stent, short-term

• Primary Device ID: 07290015518192
• NIH Device Record Key: d060eec4-b401-4abd-89b6-1aea18d56567
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iTind Removal Kit
• Version Model Number: MT-FA08
• Company DUNS: 532003626
• Company Name: MEDI-TATE LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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: 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: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com
• Phone: +972777006745
• Email: info@itind.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290015518192 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• deNovo: DEN190020

FDA Product Code

• QKA: Temporarily-Placed Urethral Opening System For Symptoms Of Benign Prostatic Hyperplasia

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: 2023-11-02
• Device Publish Date: 2023-10-25

Devices Manufactured by MEDI-TATE LTD

• 07290015518192 - iTind Removal Kit: 2023-11-02iTind Removal Kit: 1 Snare + 1 Removal Tube
• 07290015518192 - iTind Removal Kit: 2023-11-02 iTind Removal Kit: 1 Snare + 1 Removal Tube
• 07290015518062 - iTIND System: 2023-07-25 iTIND System
• 07290015518079 - iTIND: 2023-07-25
• 07290015518086 - SNARE: 2023-07-25
• 07290015518109 - iTIND System: 2023-07-25 iTIND System Box of 5
• 17290015518083 - Snare X5: 2021-07-28 Pack of 5 individually packed Snare