ASNIS 705355S

GUDID 07613327172652

Unthreaded Guide Wire JFX

Stryker Trauma SA

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile

• Primary Device ID: 07613327172652
• NIH Device Record Key: 84b29013-8ca4-40d1-ba63-af6d7d9476a0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASNIS
• Version Model Number: 705355S
• Catalog Number: 705355S
• Company DUNS: 481999654
• Company Name: Stryker Trauma SA
• 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: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0
• Length: 200 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327172652 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-07-25

On-Brand Devices [ASNIS]

• 07613327284539: Labeling Clip Implants & Instruments JFX
• 07613327284522: Screw Rack Lid JFX
• 07613327284515: Cannulated Screws Rack JFX
• 07613327284508: Labeling Clip General Instruments JFX
• 07613327284492: Screw Drawer JFX
• 07613327284485: Solid Screws Rack JFX
• 07613327284478: Instrument Rack JFX
• 07613327172867: Cannulated Screwdriver JFX
• 07613327172843: Direct Measuring Gauge JFX
• 07613327172812: Positioning Guide JFX
• 07613327172799: Sighting Arm
• 07613327172775: Double protecting sleeve JFX
• 07613327172768: Cannulated Tap JFX
• 07613327172751: Cannulated Countersink JFX
• 07613327172744: Solid Screw JFX
• 07613327172737: Cannulated Countersink JFX
• 07613327172720: Cannulated Tap JFX
• 07613327172706: Cannulated Countersink JFX
• 07613327172690: Cannulated Tap JFX
• 07613327172683: Cannulated Drill Bit JFX
• 07613327172669: Solid Screw JFX
• 07613327172652: Unthreaded Guide Wire JFX
• 07613327172645: Unthreaded Guide Wire JFX
• 07613327172638: Solid Screw JFX
• 07613327172614: Solid Screw JFX
• 07613327172607: Solid Screw JFX
• 07613327172591: Solid Screw JFX
• 07613327172577: Solid Screw JFX
• 07613327172515: Solid Screw JFX
• 07613327172508: Solid Screw JFX
• 07613327172478: Solid Screw JFX
• 07613327172461: Solid Screw JFX
• 07613327172447: Solid Screw JFX
• 07613327172430: Solid Screw JFX
• 07613327172379: Solid Screw JFX
• 07613327172362: Solid Screw JFX
• 07613327172355: Solid Screw JFX
• 07613327172348: Solid Screw JFX
• 07613327172300: Solid Screw JFX
• 07613327172287: Solid Screw JFX
• 07613327172263: Solid Screw JFX
• 07613327172249: Solid Screw JFX
• 07613327172232: Solid Screw JFX
• 07613327172195: Solid Screw JFX
• 07613327172188: Solid Screw JFX
• 07613327172164: Solid Screw JFX
• 07613327172157: Solid Screw JFX
• 07613327172126: Solid Screw JFX
• 07613327172119: Cannulated Screw JFX
• 07613327172102: Solid Screw JFX