FasTouch™ FTPC10

GUDID 17290017155118

FasTouch™ Permanent Reloadable Cartridge 10 Permanent Fasteners

VIA SURGICAL LTD

Endoscopic manual linear stapler

• Primary Device ID: 17290017155118
• NIH Device Record Key: 3001f9f9-f153-4ad8-a278-84f901fd0557
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FasTouch™
• Version Model Number: FTPC10
• Catalog Number: FTPC10
• Company DUNS: 600319250
• Company Name: VIA SURGICAL LTD
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• 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: true
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +18009696331
• Email: CS@progressivemedinc.com

Device Dimensions

• Outer Diameter: 5 Millimeter
• Length: 37 Centimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	07290017155111 [Primary]
GS1	17290017155118 [Package]; Contains: 07290017155111; Package: Box [10 Units]; In Commercial Distribution

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162252

FDA Product Code

• GDW: Staple, Implantable

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: 2018-07-06
• Device Publish Date: 2017-08-21

On-Brand Devices [FasTouch™]

• 17290017155118: FasTouch™ Permanent Reloadable Cartridge 10 Permanent Fasteners
• 07290017155104: FasTouch™ Permanent Fixation System 25 Permanent Fasteners
• 17290017155040: Sterile Sample of the FasTouch™ Permanent Reloadable Cartridge 10 Permanent Fasteners
• 17290017155019: Sterile Sample of the FasTouch™ Permanent Fixation System 25 Permanent Fasteners