Reduction Forceps, Curved, Pointed, Long Ratchet

GUDID 00848665010800

ADVANCED ORTHOPEDIC SOLUTIONS INC

Bone holding forceps

• Primary Device ID: 00848665010800
• NIH Device Record Key: 6721e191-1756-4300-bfb3-8a126cd03ae9
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Reduction Forceps, Curved, Pointed, Long Ratchet
• Version Model Number: 0901
• 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	00848665010800 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00848665010800]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-08-21
• Device Publish Date: 2016-02-26

On-Brand Devices [Reduction Forceps, Curved, Pointed, Long Ratchet]

• 00848665027396: 0901-100
• 00848665010800: 0901