Main-Knife - Alphatec 471-25-193

GUDID B90847125193

Bayonet Knife, Rigid, 193mm, Sterile

Mainstream Medical Devices, LLC

Scalpel, single-use

• Primary Device ID: B90847125193
• NIH Device Record Key: e207e9e2-000f-4fb6-9cd4-7e162843a767
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Main-Knife - Alphatec
• Version Model Number: 471-25-193
• Catalog Number: 471-25-193
• Company DUNS: 071513432
• Company Name: Mainstream Medical Devices, 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: true
• Lot Batch: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B90847125193 [Primary]

FDA Product Code

• EMF: Knife, Surgical

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-02-29
• Device Publish Date: 2024-02-21

On-Brand Devices [Main-Knife - Alphatec]

• B90845115901: Retractable Bayonet Knife, Sterile
• B90847135193: Bayonet Knife, 193MM, Sterile
• B90847125901: Single Piece Annulotomy Knife, Sterile
• B90847125193: Bayonet Knife, Rigid, 193mm, Sterile
• B9081600060: Single Piece Annulotomy Knife, Sterile