VorOtek M Scope VSMS

GUDID 09348227000160

VorOtek M Scope - SpecFrame. Plate Magnification with Fully Integrated Surgical Quality Dimmable LED Illumination. Includes 2, 4 & 6 Dioptre Plate Magnifiers, Power Pack, Charger & Carry Case.

VOROTEK PTY LTD

Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable Surgical binoculars, reusable

• Primary Device ID: 09348227000160
• NIH Device Record Key: 70d0d2a3-ab4d-4e81-aee9-32af7ad8895a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VorOtek M Scope
• Version Model Number: VSMS
• Catalog Number: VSMS
• Company DUNS: 744332997
• Company Name: VOROTEK PTY LTD
• 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: false
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	09348227000160 [Primary]

FDA Product Code

• HJH: Loupe, Binocular, Low Power

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: 2023-08-17
• Device Publish Date: 2023-08-09

On-Brand Devices [VorOtek M Scope]

• 09348227000160: VorOtek M Scope - SpecFrame. Plate Magnification with Fully Integrated Surgical Quality Dimmable
• 09348227000153: VorOtek M Scope - HeadBand. Plate Magnification with Fully Integrated Surgical Quality Dimmable