PEAK 274622000

GUDID 10705034192772

PEAK ANTERIOR COMPRESSION PLATE SYSTEM STARTER AWL

DEPUY SPINE, LLC

Bone awl, reusable

• Primary Device ID: 10705034192772
• NIH Device Record Key: 16d7b363-844d-4ea3-bda6-9a7d797c05df
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PEAK
• Version Model Number: 274622000
• Catalog Number: 274622000
• Company DUNS: 107105876
• Company Name: DEPUY SPINE, 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
• Phone: +1(800)255-2500
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	10705034192772 [Primary]

FDA Product Code

• HWJ: AWL

Sterilization

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

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

[10705034192772]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2022-06-10
• Device Publish Date: 2016-12-31

On-Brand Devices [PEAK]

• 10705034192710: PEAK ANTERIOR COMPRESSION PLATE SYSTEM HEX DRIVER INSERTER
• 10705034192772: PEAK ANTERIOR COMPRESSION PLATE SYSTEM STARTER AWL
• 10705034023663: PEAK ANTERIOR COMPRESSION PLATE SYSTEM ONE SEGMENT PLATE 22mm