Main-Knife RIGID 21mm, Alphatec 451-25-901

GUDID B90845125901

Retractable Bayonet Knife, Sterile

Mainstream Medical Devices, LLC

Scalpel, single-use

• Primary Device ID: B90845125901
• NIH Device Record Key: 9893e9e5-a246-477d-912a-99915c3ad31e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Main-Knife RIGID 21mm, Alphatec
• Version Model Number: 451-25-901
• Catalog Number: 451-25-901
• 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	B90845125901 [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: 2023-07-20
• Device Publish Date: 2023-07-12

On-Brand Devices [Main-Knife RIGID 21mm, Alphatec]

• B90845125901: Retractable Bayonet Knife, Sterile
• B9081600051: Retractable Bayonet Knife, Sterile