Flow-Drill™ 110-02-375

GUDID B267110023750

3.6 mm Flow-Drill Guide

Flow-FX

Surgical drill guide, reusable

• Primary Device ID: B267110023750
• NIH Device Record Key: acdc7d3f-67cf-4e6a-b528-9d347e8c4531
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Flow-Drill™
• Version Model Number: 110-02-375
• Catalog Number: 110-02-375
• Company DUNS: 079293587
• Company Name: Flow-FX
• 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: 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	B267110023750 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

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: 2020-12-28
• Device Publish Date: 2020-12-18

On-Brand Devices [Flow-Drill™]

• B2671101048K2: Flow-Drill 4.8mm Kit Shipper
• B2671101036K2: Flow-Drill 3.6mm Kit Shipper
• B267110023750: 3.6 mm Flow-Drill Guide
• B267110010: Ratchet Handle
• B26711000280: 2.8 mm Flow-Drill Guide Wire
• B26711000200: 2 mm Flow-Drill Guide Wire
• B26711048K0: Flow-Drill 4.8mm Kit
• B26711036K0: Flow-Drill 3.6mm Kit