1900015025

GUDID 07613327376326

2.5mm Egg Resurfacing Tool

STRYKER CORPORATION

Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use Orthopaedic bur, single-use

• Primary Device ID: 07613327376326
• NIH Device Record Key: 7565375e-690d-410b-aebd-7ab6d113ea24
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 1900015025
• Catalog Number: 1900015025
• Company DUNS: 196548481
• 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: true
• 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(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 Dimensions

• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613327376326 [Primary]

FDA Product Code

• GFF: BUR, SURGICAL, GENERAL & PLASTIC SURGERY

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-24
• Device Publish Date: 2018-09-23

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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