Hybrid MMF AXS 56-20998E

GUDID 07613327572063

Locking screw, AXS, self-drilling

Stryker Leibinger GmbH & Co. KG

Craniofacial bone screw, non-bioabsorbable

• Primary Device ID: 07613327572063
• NIH Device Record Key: e4bec14e-4892-49d5-ba24-b796e181417a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hybrid MMF AXS
• Version Model Number: 56-20998E
• Catalog Number: 56-20998E
• Company DUNS: 316153956
• Company Name: Stryker Leibinger GmbH & Co. KG
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• 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

Device Dimensions

• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0
• Length: 8 Millimeter
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327572063 [Primary]

FDA Product Code

• DZL: SCREW, FIXATION, INTRAOSSEOUS

Sterilization

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

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

[07613327572063]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-26
• Device Publish Date: 2023-09-18

On-Brand Devices [Hybrid MMF AXS]

• 07613327579789: Locking screws, AXS, self-drilling
• 07613327579765: Locking screws, AXS, self-drilling
• 07613327572070: Locking screws, AXS, self-drilling
• 07613327572056: Locking screws, AXS, self-drilling
• 07613327572063: Locking screw, AXS, self-drilling
• 07613327572049: Locking screw, AXS, self-drilling