Pitch-Patch 102-1090

GUDID 05060267133755

Tissue Reinforcement Device

XIROS LTD

Surgical support tape, non-bioabsorbable

• Primary Device ID: 05060267133755
• NIH Device Record Key: 61298bfc-303f-4688-b1ba-1d164f0d7781
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Pitch-Patch
• Version Model Number: 102-1090
• Catalog Number: 102-1090
• Company DUNS: 228209805
• Company Name: XIROS 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: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk
• Phone: +441132387202
• Email: enquiries@xiros.co.uk

Device Dimensions

• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter
• Length: 30 Millimeter
• Width: 20 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	05060267133755 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230671

FDA Product Code

• OWX: Mesh, Surgical, Non-Absorbable, Orthopaedics, Reinforcement Of Tendon

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: 2023-10-13
• Device Publish Date: 2023-10-05

On-Brand Devices [Pitch-Patch]

• 05060267132024: Tissue Reinforcement Device
• 05060267132017: Tissue Reinforcement Device
• 05060267133762: Tissue Reinforcement Device
• 05060267133755: Tissue Reinforcement Device