5805-0-225

GUDID 04546540007797

High Performance Bi-Drive Bone Drill

Stryker Trauma GmbH

Orthopaedic implantation sleeve, reusable Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible Medullary canal orthopaedic reamer, flexible

• Primary Device ID: 04546540007797
• NIH Device Record Key: e5ad4000-1f18-4a6e-9274-604bd8cec44b
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5805-0-225
• Catalog Number: 5805-0-225
• 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

• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter
• Device Size Text, specify: 0
• Length: 180 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540007797 [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

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• 07613327361803 - T2 ALPHA: 2023-06-02 Guide Wire with Ruler Tube
• 07613327406153 - T2 ALPHA: 2023-06-02 Guide Wire
• 07613327406184 - T2 ALPHA: 2023-06-02 Guide Wire
• 07613327095548 - T2: 2022-05-05 Tibia System Magnetic Trigger
• 07613153179443 - T2: 2022-02-08 Locking Screw, Fully Threaded
• 04546540202475 - T2: 2022-02-04 Locking Screw, Fully Threaded