ASY-01149

GUDID 00840200409896

9mm Open Shaver, FH7 MIS2

Integrity Implants Inc.

Bone file/rasp, manual, reusable

• Primary Device ID: 00840200409896
• NIH Device Record Key: bb17765d-0fce-4ce8-b904-ff89fe345680
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: ASY-01149
• Catalog Number: ASY-01149
• Company DUNS: 080300717
• Company Name: Integrity Implants 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: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com
• Phone: 8002019300
• Email: customerservice@integrityimplants.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840200409896 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

[00840200409896]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-04-16
• Device Publish Date: 2025-04-08

Devices Manufactured by Integrity Implants Inc.

• 00840200410656 - NA: 2025-07-25 Lock Check Handle, FH9
• 00810045530307 - FlareHawk: 2025-07-11 Shell, Short 25 mm, FH9 Sterile
• 00810045530314 - FlareHawk: 2025-07-11 Shell, Tall 25 mm, FH9 Sterile
• 00810045530321 - FlareHawk: 2025-07-11 Shell, Lordotic 25 mm, FH9 Sterile
• 00810045530338 - FlareHawk: 2025-07-11 Shell, Short 29 mm, FH9 Sterile
• 00810045530345 - FlareHawk: 2025-07-11 Shell, Tall 29 mm, FH9 Sterile
• 00810045530352 - FlareHawk: 2025-07-11 Shell, Lordotic 29 mm, FH9 Sterile
• 00810045530567 - FlareHawk: 2025-07-11 Shell, Short 26mm, FH7 Sterile