EUROStar III Plus

GUDID 04049016096795

EUROIMMUN Medizinische Labordiagnostika AG

Fluorescence light microscope

• Primary Device ID: 04049016096795
• NIH Device Record Key: dfdbb3f8-a813-4877-835f-7584bf0a06dc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EUROStar III Plus
• Version Model Number: YG 0306-0101-3
• Company DUNS: 322209263
• Company Name: EUROIMMUN Medizinische Labordiagnostika 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: false
• Serial Number: true
• Manufacturing Date: true
• 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	04049016096795 [Primary]

FDA Product Code

• KEI: Condensers, Microscope

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-09-24

Devices Manufactured by EUROIMMUN Medizinische Labordiagnostika AG

• 04049016159025 - EUROStar IV Plus: 2024-11-21
• 04049016151227 - FITC-labelled anti-human IgA: 2024-11-18
• 04049016151234 - FITC-labelled anti-human IgG: 2024-11-18
• 04049016151562 - ELISA enzyme conjugate, anti-human IgA: 2024-11-18
• 04049016151593 - FITC-labelled anti-human IgA: 2024-11-18
• 04049016151609 - FITC-labelled anti-human IgG: 2024-11-18
• 04049016137894 - IFA: Crithidia luciliae sensitive (anti-dsDNA) EUROPattern: 2024-09-19
• 04049016151999 - Mounting medium (IFA): 2024-07-25