SUBFIX XEX001001

GUDID 07613252264729

Removal Driver

Stryker Trauma SA

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable

• Primary Device ID: 07613252264729
• NIH Device Record Key: c20cab39-dd0c-4bff-ad67-94753850edb5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SUBFIX
• Version Model Number: XEX001001
• Catalog Number: XEX001001
• 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: 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	07613252264729 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

[07613252264729]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-10-02
• Device Publish Date: 2020-09-24

On-Brand Devices [SUBFIX]

• 07613252264866: Trial
• 07613252264859: Trial
• 07613252264842: Trial
• 07613252264835: Trial
• 07613252264828: Trial
• 07613252263531: Arthroeresis Implant
• 07613252263524: Arthroeresis Implant
• 07613252263517: Arthroeresis Implant
• 07613252263500: Arthroeresis Implant
• 07613252263494: Arthroeresis Implant
• 07613252266990: Insertion Driver
• 07613252266754: Ancillary Set
• 07613252266433: Tray with Lid
• 07613252264729: Removal Driver
• 07613252264545: Guidewire