Instrument Set (Case and Reusable Instruments) CIS-003

GUDID 10855068008522

A custom engineered set of reusable surgical instruments, housed in a sterilizable storage container, that are used during a CurvaFix surgical procedure.

Curvafix Inc

Orthopaedic surgical procedure kit, non-medicated, reusable

• Primary Device ID: 10855068008522
• NIH Device Record Key: 72b3ae83-d3bd-4187-bc62-1288a25629bc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Instrument Set (Case and Reusable Instruments)
• Version Model Number: CIS-003
• Catalog Number: CIS-003
• Company DUNS: 039779098
• Company Name: Curvafix Inc
• 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com
• Phone: 425-276-8800
• Email: support@curvafix.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10855068008522 [Primary]

FDA Product Code

• HSB: Rod, Fixation, Intramedullary And Accessories

Sterilization

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

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

[10855068008522]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-06-28
• Device Publish Date: 2022-06-20

On-Brand Devices [Instrument Set (Case and Reusable Instruments)]

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• 10855068008737: A custom engineered set of reusable surgical instruments, housed in a sterilizable storage conta