SONICFUSION 1910-2611S

GUDID 07613252495147

Drill SonicPin

Stryker Trauma GmbH

Fluted surgical drill bit, single-use, sterile Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use Fluted surgical drill bit, single-use

• Primary Device ID: 07613252495147
• NIH Device Record Key: c0e22c3c-223c-47b8-81d0-3277998a9e63
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONICFUSION
• Version Model Number: 1910-2611S
• Catalog Number: 1910-2611S
• Company DUNS: 330211587
• Company Name: Stryker Trauma GmbH
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Dimensions

• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0
• Length: 26 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613252495147 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-15
• Device Publish Date: 2020-04-07

On-Brand Devices [SONICFUSION]

• 07613327129649: Instrument Tray
• 07613327096071: TipTool
• 07613327096033: TipTool
• 07613327096019: Handpiece
• 07613327095470: Handpiece Tip
• 07613327095463: Handpiece Tip
• 07613327095418: Drill
• 07613327095371: Drill
• 07613252495116: Instrument Tray SonicPin
• 07613252495093: Foot Switch
• 07613252495086: Handpiece SonicPin
• 07613252495079: Ultrasonic Generator
• 07613252495161: Direct Depth Gauge SonicPin
• 07613252495154: Drill cannulated SonicPin (Pin26mm)
• 07613252495147: Drill SonicPin
• 07613252495123: Drill cannulated SonicPin
• 07613252212348: Drill SonicPin