03311047

GUDID H679033110470

REDUCTION WIRE 1.8MM DIA HALF POINT TIP

Synthes GmbH

Orthopaedic bone wire

• Primary Device ID: H679033110470
• NIH Device Record Key: 31cceb08-3cf0-49c3-8144-8ee34bde5e15
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.311.047
• Catalog Number: 03311047
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886982078063 [Primary]
HIBCC	H679033110470 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092190

FDA Product Code

• KTT: APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

Sterilization

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

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

[H679033110470]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-05-27
• Device Publish Date: 2015-09-14

Devices Manufactured by Synthes GmbH

• 07612334270139 - EXPert Nail: 2025-10-02 TRAY F/TIBIAL NAIL EX SP INSTR
• H679310930 - NA: 2025-10-01 SMALL CHUCK WITH KEY
• 10886982350190 - NA: 2025-09-22 2.0MM STRAIGHT PLATE 20 HOLES
• 10887587078465 - NA: 2025-09-19 NONRETAINING SCREWDRIVER BLADE FOR 90DEG SCREWDRIVER
• 10886982349873 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 16MM
• 10886982349880 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 18MM
• 10886982349897 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 20MM
• 10886982349903 - NA: 2025-09-01 CANNULATED CIRCULAR REAMER 22MM