GRYPHON 211037

GUDID 10886705001491

GRYPHON Fishmouth Guide

DEPUY MITEK, LLC

Orthopaedic guidewire, reusable

• Primary Device ID: 10886705001491
• NIH Device Record Key: 1b008439-e067-44a7-824c-b1b76d107d7f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GRYPHON
• Version Model Number: 211037
• Catalog Number: 211037
• Company DUNS: 190572854
• Company Name: DEPUY MITEK, LLC
• 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

Customer Support Contacts

• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705001491 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

[10886705001491]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2023-09-18
• Device Publish Date: 2015-09-01

On-Brand Devices [GRYPHON]

• 10886705001484: GRYPHON DRILL BIT
• 10886705001477: GRYPHON TAP
• 10886705024131: GRYPHON Slotted Fishmouth Guide
• 10886705024063: GRYPHON Slotted Sawtooth Guide
• 10886705021116: GRYPHON Hip Guide Fishmouth
• 10886705021109: GRYPHON Hip Guide Sawtooth
• 10886705001514: GRYPHON Sawtooth Guide
• 10886705001491: GRYPHON Fishmouth Guide