Omnia Medical PsiF 01-5P-ADP1

GUDID 00843511121242

Drill Adapter

OMNIA MEDICAL, LLC

Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant/instrument adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable Orthopaedic implant-instrument extension adaptor, reusable

• Primary Device ID: 00843511121242
• NIH Device Record Key: 85e62c34-43d7-4c4c-a9e7-17ff34f22c5d
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Omnia Medical PsiF
• Version Model Number: 01-5P-ADP1
• Catalog Number: 01-5P-ADP1
• Company DUNS: 079467378
• Company Name: OMNIA MEDICAL, 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: true

Customer Support Contacts

• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com
• Phone: 3044134851
• Email: customerservice@omniamedical.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00843511121242 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

[00843511121242]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-10-25
• Device Publish Date: 2021-10-15

On-Brand Devices [Omnia Medical PsiF]

• 00843511100681: PsiF Impaction Cap Ball Handle
• 00843511100674: PsiF Joint Finder Instrument
• 00843511100667: PsiF Cannula Instrument
• 00843511100650: PsiF Box Cutter Rasp Instrument
• 00843511100643: PsiF Slap Hammer Peg Instrument
• 00843511100636: PsiF Post Packer (Long Impactor) Instrument
• 00843511100629: PsiF Allograft Inserter Instrument
• 00843511101251: PsiF Impaction Cap Handle
• 00843511100902: Orthocision PsiF Box Cutter
• 00843511101336: 1.4 mm x 130 mm Kwire
• 00843511121778: Kwire, 1.4mm x 460 mm Nitinol, blunt drill
• 00843511121266: Impaction Cap Handle
• 00843511121228: Joint finder
• 00843511121242: Drill Adapter