FORUM ASSIST match

GUDID 04049471070200

Carl Zeiss Meditec AG

Patient health record information system application software

• Primary Device ID: 04049471070200
• NIH Device Record Key: 26d28717-4a13-4bfc-a562-3ed4cd495dba
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FORUM ASSIST match
• Version Model Number: 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	04049471070200 [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: 2021-04-21
• Device Publish Date: 2021-04-13

On-Brand Devices [FORUM ASSIST match]

• 04049471000037: This database entry covers UDI for SW Versions 1.4.1 and higher: (01)04049471000037(10)150 -> Ve
• 04049471100037: This database entry covers UDI for SW Versions 1.4.1 and higher: (01)04049471000037(10)150-> Ver
• 04049471070200: 1