ANTERION

GUDID 04059237000945

Heidelberg Engineering GmbH

Eye anterior segment analyser

• Primary Device ID: 04059237000945
• NIH Device Record Key: 7d9efefb-7be8-4d3a-a414-e7d6f4567d18
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ANTERION
• Version Model Number: Software V.1.2.4 US
• Company DUNS: 329833875
• Company Name: Heidelberg Engineering GmbH
• 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: false
• 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	04059237000945 [Primary]

FDA Product Code

• OBO: Tomography, Optical Coherence

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: 2023-11-27
• Device Publish Date: 2023-11-18

On-Brand Devices [ANTERION]

• 04059237000617: 88036
• 04059237000754: Software with HEYEX 2 V1.2.3
• 04059237000877: 88036
• 04059237000945: Software V.1.2.4 US
• 04059237000938: 88036