ROSA® Registration Pointer 20-8020-013-00

GUDID 00887868581083

Orthosoft Inc

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 00887868581083
• NIH Device Record Key: 72730fc7-bd9e-4408-b999-b6b4e2c04683
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ROSA® Registration Pointer
• Version Model Number: 20-8020-013-00
• Catalog Number: 20-8020-013-00
• Company DUNS: 205670032
• Company Name: Orthosoft Inc
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: true
• 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	00887868581083 [Primary]

FDA Product Code

• OLO: Orthopedic stereotaxic instrument

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2026-03-02
• Device Publish Date: 2026-02-20

On-Brand Devices [ROSA® Registration Pointer]

• 00889024505230: 20-8020-013-00
• 00887868581083: 20-8020-013-00