TransFasten - LSF, General Instrument Tray

GUDID M739102900109

Sterilization Case - General Instrument Tray

CAPTIVA SPINE, INC.

Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable

• Primary Device ID: M739102900109
• NIH Device Record Key: d2b3db91-1ab1-41b2-985b-34186a6b7ac4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TransFasten - LSF, General Instrument Tray
• Version Model Number: 10-2-9001
• Company DUNS: 836975784
• Company Name: CAPTIVA SPINE, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com
• Phone: 561-277-9480
• Email: info@captivaspine.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M739102900109 [Primary]

FDA Product Code

• FSM: Tray, Surgical, Instrument

Sterilization

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

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

[M739102900109]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-05-03
• Device Publish Date: 2024-04-25

Devices Manufactured by CAPTIVA SPINE, INC.

• M739102900109 - TransFasten - LSF, General Instrument Tray: 2024-05-03Sterilization Case - General Instrument Tray
• M739102900109 - TransFasten - LSF, General Instrument Tray: 2024-05-03 Sterilization Case - General Instrument Tray
• M73910290020 - TransFasten - LSF, Quick Connect Drill: 2024-05-03 Quick Connect Drill
• M73910290030 - TransFasten-LSF, Tissue Protector: 2024-05-03 Tissue Protector
• M73910290050 - TransFasten-LSF, Implant Driver Shaft: 2024-05-03 Implant Driver Shaft
• M73910290060 - TransFasten-LSF, Offset Guide: 2024-05-03 Offset Guide
• M73910290070 - TransFasten-LSF, Tissue Dilator: 2024-05-03 Tissue Dilator
• M739102901009 - TransFasten-LSF, Plunger Rod: 2024-05-03 Plunger Rod
• M73910290110 - TransFasten - LSF, Implant Filling Tube: 2024-05-03 Implant Filling Tube