NEOSYS

GUDID 03760225713006

IN2BONES

Orthopaedic surgical procedure kit, non-medicated, single-use

• Primary Device ID: 03760225713006
• NIH Device Record Key: 616e0cd0-a3e0-433c-bca2-2660557fe9c1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: NEOSYS
• Version Model Number: G02 10011
• Company DUNS: 263616749
• Company Name: IN2BONES
• 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: 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: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com
• Phone: +33472292626
• Email: contact@in2bones.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	03760225713006 [Primary]

FDA Product Code

• KDD: Kit, Surgical Instrument, Disposable

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: 2022-05-18
• Device Publish Date: 2022-05-10

On-Brand Devices [NEOSYS]

• 03760225712191: G02 10001
• 03760225713006: G02 10011
• 03701337606275: NEOSYS SINGLE USE SET COMPLETE
• 03701337606213: NEOSYS SINGLE USE SET FOOT 3.0-3.5 DMMO
• 03701337606206: NEOSYS SINGLE USE SET FOOT 2.0-2.5 DMMO
• 03701337606190: NEOSYS SINGLE USE SET FOOT DMMO
• 03701337606183: NEOSYS SINGLE USE SET FOOT 3.0-3.5 DRILL "L"
• 03701337606176: NEOSYS SINGLE USE SET FOOT 2.0-2.5 DRILL "M"
• 03701337606169: NEOSYS SINGLE USE SET FOOT 3.0-3.5 CANN DRILL "L"
• 03701337606152: NEOSYS SINGLE USE SET FOOT 2.0-2.5 CANN DRILL "M"
• 03701337606145: NEOSYS SINGLE USE SET FOOT 3.0-3.5 CANN DRILL "S"
• 03701337606138: NEOSYS SINGLE USE SET HAND 2.0-2.5 CANN DRILL "S"
• 03701337606121: NEOSYS SINGLE USE SET FOOT 2.0-2.5 CANN DRILL "S"
• 03701337606114: NEOSYS SINGLE USE SET FOOT 3.0-3.5
• 03701337606107: NEOSYS SINGLE USE SET HAND 2.0-2.5
• 03701337606091: NEOSYS SINGLE USE SET FOOT 2.0-2.5