05001120

GUDID 07611819813717

DRILL ATTACHMENT W/JACOBS CHUCK FOR PEN DRIVE

Synthes GmbH

Surgical drill chuck

• Primary Device ID: 07611819813717
• NIH Device Record Key: 4f406536-81fe-41fe-8c1a-bf307d2760bf
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 05.001.120
• Catalog Number: 05001120
• 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	07611819813717 [Direct Marking]
GS1	10886982129345 [Primary]
HIBCC	H679050011200 [Secondary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K043310

FDA Product Code

• DZI: DRILL, BONE, POWERED

Sterilization

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

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

[07611819813717]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2022-04-18
• Device Publish Date: 2016-06-30

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