Mobio™ Specialty 8829P03080

GUDID 00843575124586

Femoral Impactor- Notch Type

B-ONE ORTHO, CORP.

Orthopaedic implant impactor, reusable

• Primary Device ID: 00843575124586
• NIH Device Record Key: 1373cb68-caf2-4c6e-8ea1-326237865bf7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mobio™ Specialty
• Version Model Number: 8829P03080
• Catalog Number: 8829P03080
• Company DUNS: 081315444
• Company Name: B-ONE ORTHO, CORP.
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843575124586 [Primary]

FDA Product Code

• HWA: Impactor

Sterilization

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

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

[00843575124586]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-02-05
• Device Publish Date: 2025-01-28

On-Brand Devices [Mobio™ Specialty ]

• 00843575120304: Tibial Insert Trial Impactor/Extractor
• 00843575120298: PR Sizer Impactor
• 00843575120281: Pin Driver
• 00843575119131: PR Shift Block
• 00843575124586: Femoral Impactor- Notch Type
• 00843575122650: Distal Femoral Alignment Guide
• 00843575124579: TIBIAL TRIAL PLATE, SIZE J
• 00843575124562: TIBIAL TRIAL PLATE, SIZE H
• 00843575124555: TIBIAL TRIAL PLATE, SIZE G
• 00843575124548: TIBIAL TRIAL PLATE, SIZE F
• 00843575124531: TIBIAL TRIAL PLATE, SIZE E
• 00843575124524: TIBIAL TRIAL PLATE, SIZE D
• 00843575124517: TIBIAL TRIAL PLATE, SIZE C
• 00843575124500: TIBIAL TRIAL PLATE, SIZE B
• 00843575124487: TIBIAL PLATE TRIAL HANDLE