Hana/ProFx Femoral Hook Left 6850-919

GUDID 00842430106828

MIZUHO ORTHOPEDIC SYSTEMS, INC.

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• Primary Device ID: 00842430106828
• NIH Device Record Key: c0c3eaa0-1496-4a3b-92f6-e75e1300b46f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hana/ProFx Femoral Hook Left
• Version Model Number: 6850-919
• Catalog Number: 6850-919
• Company DUNS: 084527241
• Company Name: MIZUHO ORTHOPEDIC SYSTEMS, 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com
• Phone: 1-800-777-4674
• Email: CustServ@mizuhosi.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00842430106828 [Primary]

FDA Product Code

• LHX: Trousers, Anti-Shock
• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

[00842430106828]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-12-28
• Device Publish Date: 2018-11-27

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• 00842430101311 - SPAR,LEG,RIGHT RADIOLUCENT,REFURBISHED: 2023-09-27
• 00842430101328 - SPAR, LEG, LEFT, RADIOLUCENT, REFURBISHED: 2023-09-27
• 00842430101335 - SPAR ASSEMBLY, RIGHT, REFURBISHED: 2023-09-27
• 00842430101342 - SPAR ASSEMBLY, LEFT, REFURBISHED: 2023-09-27
• 00842430103414 - UPPER ARM SUPPORT & PAD, REFURBISHED: 2023-09-27