KNOTILUS+ 3911-124-408

GUDID 07613327623796

2.4X8.9MM DRILL, HIP

STRYKER CORPORATION

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• Primary Device ID: 07613327623796
• NIH Device Record Key: 3a15e015-2e93-4f0e-beae-8ee4af29099e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: KNOTILUS+
• Version Model Number: 3911124408
• Catalog Number: 3911-124-408
• Company DUNS: 187502109
• Company Name: STRYKER CORPORATION
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx
• Phone: +1(866)624-4422
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327623796 [Primary]

FDA Product Code

• HTW: BIT, DRILL

Sterilization

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

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

[07613327623796]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-03-13
• Device Publish Date: 2024-03-05

On-Brand Devices [KNOTILUS+]

• 07613327623826: PENCIL TIP OBTURATOR
• 07613327623819: OFFSET TIP GUIDE
• 07613327623758: FISHMOUTH TIP GUIDE
• 07613327623734: FORK TIP GUIDE, HIP
• 07613327623727: CROWN TIP GUIDE
• 07613327623710: BULLET TIP OBTURATOR, CANNULATED
• 07613327623680: PENCIL TIP OBTURATOR, HIP
• 07613327623666: CROWN TIP GUIDE, HIP
• 07613327623659: BULLET TIP OBTURATOR, CANNULATED, HIP
• 07613327627657: 2.9X12.5MM KNOTILUS+ ANCHOR - PEEK
• 07613327627640: 2.9X15.5MM KNOTILUS+ ANCHOR - PEEK
• 07613327627633: 2.4X11.3MM KNOTILUS+ ANCHOR - PEEK
• 07613327623833: 2.4X8.9MM DRILL, HARD BONE, HIP
• 07613327623796: 2.4X8.9MM DRILL, HIP
• 07613327627701: 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
• 07613327627664: 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK