FORUM

GUDID 04049471070026

This database entry covers UDI for SW Versions 4.1 and higher: (01)04049471070026(10)411 -> Version 4.1.1; (01)04049471070026(10)420 -> Version 4.2; (01)04049471070026(10)421 -> Version 4.2.1; (01)04049471070026(10)423 -> Version 4.2.3; (01)04049471070026(10)424 -> Version 4.2.4

Carl Zeiss Meditec AG

Patient health record information system application software

• Primary Device ID: 04049471070026
• NIH Device Record Key: 491353d8-bf47-4543-9fbc-a4092fd82dc4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORUM
• Version Model Number: 4.1
• Company DUNS: 314594680
• 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: false
• 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	04049471070026 [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: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2019-07-11
• Device Publish Date: 2016-09-16

On-Brand Devices [FORUM]

• 04049471070026: This database entry covers UDI for SW Versions 4.1 and higher: (01)04049471070026(10)411 -> Vers
• 04049471070330: Intended Use: FORUM is a software system intended for use in storage, management, processing, a