04305010

GUDID H980043050100

2.5MM/4.0MM TI SELF-DRILLING SCHANZ SCREW 50MM

SYNTHES (U.S.A.) LP

Orthopaedic bone screw, non-bioabsorbable, non-sterile

• Primary Device ID: H980043050100
• NIH Device Record Key: 08450a1d-d9f6-45ae-8275-545ccca03ead
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 04.305.010
• Catalog Number: 04305010
• Company DUNS: 832637081
• Company Name: SYNTHES (U.S.A.) LP
• 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: 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(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10887587015125 [Primary]
HIBCC	H980043050100 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K040169

FDA Product Code

• MQN: EXTERNAL MANDIBULAR FIXATOR AND/OR DISTRACTOR

Sterilization

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

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

[H980043050100]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2015-09-14

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• H6792042360 - NA: 2024-07-24 3.5MM SHAFT SCREW 36MM
• H6792042380 - NA: 2024-07-24 3.5MM SHAFT SCREW 38MM