Mini-Blade® BEAVER6700

GUDID 00886158004417

Mini-Blade®

Beaver-Visitec International, Inc.

Manual scalpel blade, single-use

• Primary Device ID: 00886158004417
• NIH Device Record Key: 8ce28334-9f41-4b49-be1f-f7dd5f8f9e77
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mini-Blade®
• Version Model Number: BEAVER6700
• Catalog Number: BEAVER6700
• Company DUNS: 001406024
• Company Name: Beaver-Visitec International, Inc.
• Device Count: 20
• 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: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com
• Phone: 18669068080
• Email: customersupport@beaver-visitec.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00886158004417 [Unit of Use]
GS1	30886158004418 [Primary]

FDA Product Code

• GES: Blade, Scalpel

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: 2022-02-22
• Device Publish Date: 2022-02-14

On-Brand Devices [Mini-Blade®]

• 00886158004431: LAMELLAR BLADE 60 DEGREES BEVEL-UP (3EA)
• 00886158004417: Mini-Blade®
• 30886158001073: BLADE 5.0MM CUTTING W S/SU (3/SP)
• 30886158000724: KNIFE MINI SHARP ALL AROUND S/SU (10/SP)