03010503

GUDID H679030105030

13.0MM PROTECTION SLEEVE FOR RAFN ANTEGRADE/QC

Synthes GmbH

Orthopaedic implantation sleeve, reusable

• Primary Device ID: H679030105030
• NIH Device Record Key: 8f28a8bf-131f-495d-afd5-1e41f355b9e9
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 03.010.503
• Catalog Number: 03010503
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	07611819499003 [Direct Marking]
GS1	10886982069207 [Primary]
HIBCC	H679030105030 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K033618

FDA Product Code

• HSB: ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Sterilization

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

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

[H679030105030]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2022-04-28
• Device Publish Date: 2015-09-14

Devices Manufactured by Synthes GmbH

• 10886982313690 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 3H/93MM
• 10886982313706 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 3H/93MM/STERILE
• 10886982313713 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 5H/119MM
• 10886982313720 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 5H/119MM/STERILE
• 10886982313737 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 3H/93MM
• 10886982313744 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 3H/93MM/STERILE
• 10886982313751 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 5H/119MM
• 10886982313768 - VOLT: 2025-04-03 3.5 VOLT(TM) PROX HUM PLATE 5H/119MM/STERILE