CALLISTO eye

GUDID 04049539104366

Carl Zeiss Meditec AG

Operating room audiovisual data/device management system

• Primary Device ID: 04049539104366
• NIH Device Record Key: 92085500-3766-4ebd-bde0-4041b8cb679a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CALLISTO eye
• Version Model Number: CALLISTO eye
• Company DUNS: 342228620
• Company Name: Carl Zeiss Meditec AG
• 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: false
• 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	04049539104366 [Primary]

FDA Product Code

• NFJ: System, Image Management, Ophthalmic

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: 2018-09-17
• Device Publish Date: 2018-08-17

On-Brand Devices [CALLISTO eye]

• 04049539104366: CALLISTO eye
• 04049539102423: 3.2.1
• 04049539069092: 3.5.1