arcad® 2.0 XFP01013

GUDID 03700879516585

Extraction forceps

NOVASTEP

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
• 03700879516479: Akin Compressive staple Duo 10x10x12