FORUM Viewer App

GUDID 04049471100020

Carl Zeiss Meditec AG

Patient health record information system application software

• Primary Device ID: 04049471100020
• NIH Device Record Key: 0189bdf9-f20e-4b52-accc-b6150d68bf7c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORUM Viewer App
• Version Model Number: FORUM Viewer App
• Company DUNS: 314594680
• Company Name: Carl Zeiss Meditec AG
• 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: 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	04049471100020 [Primary]

FDA Product Code

• NFG: Device, Communications, Images, 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: 2018-04-23
• Device Publish Date: 2018-03-22

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• 04049539106766 - Single-use lenses for RESIGHT, ULTRA WIDE-ANGLE LENS: 2024-11-15 Single- use lenses for RESIGHT are ophthalmic surgical microscope lenses used in combination with the ZEISS RESIGHT fundus viewi
• 04049539064097 - KINEVO 900 S: 2024-10-15
• 04049539070159 - BLUE 400: 2024-10-15 accessory for surgical microscopes
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