AOS PIN GUIDE 3.2mm

GUDID 00848665001310

ADVANCED ORTHOPEDIC SOLUTIONS INC

Orthopaedic implantation sleeve, reusable

• Primary Device ID: 00848665001310
• NIH Device Record Key: 82c9bc28-b933-4c3e-9c2f-3f0a8a1978cf
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AOS PIN GUIDE 3.2mm
• Version Model Number: 0303-200
• Company DUNS: 117858154
• Company Name: ADVANCED ORTHOPEDIC SOLUTIONS INC
• 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: true
• 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	00848665001310 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00848665001310]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-12-21

On-Brand Devices [AOS PIN GUIDE 3.2mm]

• 00848665014143: 0335
• 00848665010664: 0312-200
• 00848665001488: 0319
• 00848665001310: 0303-200