Bone Screw 9069.50.075

GUDID 08033390026871

Drill Guide - Dia. 4.5 mm

LIMACORPORATE SPA

Surgical drill guide, reusable

• Primary Device ID: 08033390026871
• NIH Device Record Key: 6aa84f99-a290-4375-ac43-041199baa1a5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Bone Screw
• Version Model Number: 9069.50.075
• Catalog Number: 9069.50.075
• Company DUNS: 432066322
• Company Name: LIMACORPORATE SPA
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08033390026871 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[08033390026871]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-04-06
• Device Publish Date: 2018-09-21

On-Brand Devices [Bone Screw]

• 08033390114523: Acetabular Drilling Guide
• 08033390026871: Drill Guide - Dia. 4.5 mm
• 08033390179614: Short exagonal Screwdriver 2,5 mm