GRYPHON 213042

GUDID 10886705021109

GRYPHON Hip Guide Sawtooth

DEPUY MITEK, LLC

Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable Orthopaedic guidewire, reusable

• Primary Device ID: 10886705021109
• NIH Device Record Key: a5c59a0d-fdbd-4de2-9236-02311a165198
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GRYPHON
• Version Model Number: 213042
• Catalog Number: 213042
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	10886705021109 [Primary]

FDA Product Code

• LXH: ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

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

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

Moist Heat or Steam Sterilization

[10886705021109]

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