Arvis 804-33-005

GUDID 00860012987801

Quantum Ops, Inc.

Arm procedure positioner, reusable

• Primary Device ID: 00860012987801
• NIH Device Record Key: b7af5c6f-1981-444c-97a2-df220e105730
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Arvis
• Version Model Number: Arvis C Tracker Mount
• Catalog Number: 804-33-005
• Company DUNS: 036253884
• Company Name: Quantum Ops, Inc.
• Device Count: 1
• DM Exempt: true
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00860012987801 [Primary]

FDA Product Code

• BWN: Table And Attachments, Operating-Room

Sterilization

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

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

[00860012987801]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-11-20
• Device Publish Date: 2024-11-12