BALL NOSE GUIDE WIRE PACK OF 10 0101-900S

GUDID 10848665000044

ADVANCED ORTHOPAEDIC SOLUTIONS, INC.

Orthopaedic bone wire

• Primary Device ID: 10848665000044
• NIH Device Record Key: ea275950-91a2-4418-ae76-bf5d32d606b2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BALL NOSE GUIDE WIRE PACK OF 10
• Version Model Number: PK0101-900S
• Catalog Number: 0101-900S
• Company DUNS: 117858154
• Company Name: ADVANCED ORTHOPAEDIC 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: true
• 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	10848665000044 [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: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2021-04-30
• Device Publish Date: 2016-03-07

Devices Manufactured by ADVANCED ORTHOPAEDIC SOLUTIONS, INC.

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• 00848665035667 - TARGETER ALIGNMENT LOCK: 2026-01-26