AUTOFIX 903-0054

GUDID 03700586903050

Cannulated T handle quick coupling

Stryker GmbH

Surgical instrument handle, non-torque-limiting

• Primary Device ID: 03700586903050
• NIH Device Record Key: 01beedde-4e2a-48cb-a08d-4976ad80435d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AUTOFIX
• Version Model Number: 903-0054
• Catalog Number: 903-0054
• Company DUNS: 481999654
• Company Name: Stryker GmbH
• Device Count: 1
• DM Exempt: true
• 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: 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	03700586903050 [Primary]

FDA Product Code

• HXX: SCREWDRIVER

Sterilization

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

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

[03700586903050]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-04-14
• Device Publish Date: 2018-09-21

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