GENESIS AWL 40AWL055

GUDID 00850005827313

AWL, 5.5MM

Genesis Biologics, Inc.

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• Primary Device ID: 00850005827313
• NIH Device Record Key: 58143006-ff85-4857-b059-9d00907fdca2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GENESIS AWL
• Version Model Number: 40AWL055
• Catalog Number: 40AWL055
• Company DUNS: 016463487
• Company Name: Genesis Biologics, Inc.
• 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: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: (657) 888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850005827313 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

[00850005827313]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-03-24
• Device Publish Date: 2023-03-16

On-Brand Devices [GENESIS AWL]

• 00850005827313: AWL, 5.5MM
• 00850005827306: AWL, 4.5MM