Instrument 260-101-017

GUDID 00813110023902

Reamer Removal Wrench

BICON, LLC

Surgical instrument handle, non-torque-limiting Surgical instrument handle, non-torque-limiting

• Primary Device ID: 00813110023902
• NIH Device Record Key: 849fb41d-0f35-4a98-9d2c-6dd83826b389
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Instrument
• Version Model Number: 260-101-017
• Catalog Number: 260-101-017
• Company DUNS: 945015758
• Company Name: BICON, 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: true
• 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
GS1	00813110023902 [Primary]

FDA Product Code

• DZN: Instruments, Dental Hand

Sterilization

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

[00813110023902]

Moist Heat or Steam Sterilization

[00813110023902]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-03-24
• Device Publish Date: 2016-09-19

On-Brand Devices [Instrument]

• 00813110027399: Attachment Gauge
• 00813110024619: Straight Stealth Latch Driver
• 00813110023957: Hex Screwdriver
• 00813110023902: Reamer Removal Wrench
• 00813110028990: Hex Screwdriver, 20mm
• 00813110028556: FDUA Latch Driver
• 00813110029539: Mesh Screwdriver