5100-015-251

GUDID 04546540384942

Micro Drill Attachment Irrigation Clip

STRYKER CORPORATION

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• Primary Device ID: 04546540384942
• NIH Device Record Key: 70938a25-e225-4c15-9a91-b1471c098218
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5100015251
• Catalog Number: 5100-015-251
• Company DUNS: 196548481
• Company Name: STRYKER CORPORATION
• 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: 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

Customer Support Contacts

• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com
• Phone: +1(800)253-3210
• Email: Inst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	04546540384942 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032117

FDA Product Code

• EIA: UNIT, OPERATIVE DENTAL

Sterilization

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

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

[04546540384942]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-01-20
• Device Publish Date: 2018-09-24

Devices Manufactured by STRYKER CORPORATION

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• 07613327627664 - KNOTILUS+: 2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK
• 07613327627701 - KNOTILUS+: 2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
• 07613327623796 - KNOTILUS+: 2024-03-13 2.4X8.9MM DRILL, HIP
• 07613327623833 - KNOTILUS+: 2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
• 07613327634686 - Iconix: 2024-03-12 Iconix DC Guide for 1.4mm anchor
• 07613327634693 - Iconix: 2024-03-12
• 07613327616675 - SPY: 2024-03-06