314743

GUDID 07611819739208

DRIVE SHAFT-MINIMUM 520MM LENGTH-FOR USE WITH RIA

Synthes GmbH

Medullary canal orthopaedic reamer, flexible

• Primary Device ID: 07611819739208
• NIH Device Record Key: f685f5e2-1d1b-4ec8-8768-088b23ac51c0
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 314.743
• Catalog Number: 314743
• Company DUNS: 486711679
• Company Name: Synthes GmbH
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07611819739208 [Direct Marking]
GS1	10886982189042 [Primary]
HIBCC	H6793147430 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K013527

FDA Product Code

• HRX: ARTHROSCOPE

Sterilization

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

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

[07611819739208]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-04-29
• Device Publish Date: 2016-06-30

Devices Manufactured by Synthes GmbH

• 10887587078427 - NA: 2025-02-28 1.85MM ORTHOGNATHIC TAP
• 10886982344410 - NA: 2025-02-26 MAXFRAME CONTROL BOX TEMPLATE
• 10886982348333 - NA: 2025-02-26 1.1MM PARALLEL WIRE GUIDE
• 10886982348364 - NA: 2025-02-26 1.4MM PARALLEL WIRE GUIDE
• 10886982348395 - NA: 2025-02-26 1.6MM PARALLEL WIRE GUIDE
• 10886982349088 - NA: 2025-02-26 TERMITE REDUCTION FORCEPS SERRATED JAW
• H6792050550 - NA: 2025-02-20 3.5MM CANNULATED SCREW PARTIALLY THREADED/55MM
• H6794089050 - NA: 2025-02-20 7.3MM TI CANNULATED SCREW 16MM THREAD/105MM