5100020200

GUDID 04546540075222

Quantum Drill Irrigation Clip

STRYKER CORPORATION

Sawing power tool attachment, oscillating

• Primary Device ID: 04546540075222
• NIH Device Record Key: 599aabb9-9a6f-4d64-a266-b24c712a949c
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 5100020200
• Catalog Number: 5100020200
• 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	04546540075222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K032117

FDA Product Code

• DZI: DRILL, BONE, POWERED

Sterilization

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

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

Moist Heat or Steam Sterilization

[04546540075222]

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: 2016-09-23

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• 07613327578584 - Target Tetra: 2024-10-08 Detachable Coil
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• 07613327578607 - Target Tetra: 2024-10-08 Detachable Coil