arcad® 2.0 XFP01013

GUDID 03700879516585

Extraction forceps

NOVASTEP

General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit General internal orthopaedic fixation system implantation kit

• Primary Device ID: 03700879516585
• NIH Device Record Key: a0c3d2ba-cdaf-44dd-87f2-24249395649c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: arcad® 2.0
• Version Model Number: XFP01013
• Catalog Number: XFP01013
• Company DUNS: 264255288
• Company Name: NOVASTEP
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com
• Phone: +33299338650
• Email: contact@novastep-ortho.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700879516585 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

[03700879516585]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-04-24
• Device Publish Date: 2024-04-16

On-Brand Devices [arcad® 2.0]

• 03700879516585: Extraction forceps
• 03700879516561: Trial Sizer
• 03700879516554: MTP Compressive staple Quadro 30x16x16x14x12
• 03700879516547: Compressive staple Quadro 30x20
• 03700879516530: Compressive staple Quadro 26x18
• 03700879516523: Compressive staple Duo 25x20
• 03700879516516: Compressive staple Duo 20x20
• 03700879516509: Compressive staple Duo 18x18
• 03700879516493: Compressive staple Duo 15x15
• 03700879516486: Compressive staple Duo 12x12