Bayonet Monopolar Forceps B68810

GUDID B089B688100

CUSHING BAYONET MONOPOLAR FORCEPS; 8"(20CM)

BLACK & BLACK SURGICAL, INC.

Open-surgery electrosurgical electrode, monopolar, reusable

• Primary Device ID: B089B688100
• NIH Device Record Key: 0f1dbe18-c6b5-4b28-a585-ca05f0489ee4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bayonet Monopolar Forceps
• Version Model Number: B68810
• Catalog Number: B68810
• Company DUNS: 004382282
• Company Name: BLACK & BLACK SURGICAL, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false

Customer Support Contacts

• Phone: 877-252-2517
• Email: info@blackandblacksurgical.com
• Phone: 877-252-2517
• Email: info@blackandblacksurgical.com

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B089B688100 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K072124

FDA Product Code

• GEI: Electrosurgical, Cutting & Coagulation & Accessories

Sterilization

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

[B089B688100]

Moist Heat or Steam Sterilization

[B089B688100]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-09-20

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