Headed Screw System Instruments T009000040

GUDID 00810030824602

2.5 Headed Screw Countersink

Tyber Medical LLC

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: 00810030824602
• NIH Device Record Key: e0caa0e8-07a4-44fa-8d2f-d9ab4cf48d5b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Headed Screw System Instruments
• Version Model Number: T009000040
• Catalog Number: T009000040
• Company DUNS: 010968002
• Company Name: Tyber Medical LLC
• 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: 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: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com
• Phone: +1(866)761-0933
• Email: jstigliano@tybermed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00810030824602 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

[00810030824602]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-01-22
• Device Publish Date: 2020-01-14

On-Brand Devices [Headed Screw System Instruments]

• 00810030825029: Ø1.5 / Ø2.0 / Ø2.5 Screw Caddy – Short Thread
• 00810030824602: 2.5 Headed Screw Countersink
• 00810030824596: 2.0 Headed Screw Countersink