EUROLabLiquidHandler (30-10)

GUDID 04049016109754

EUROIMMUN Medizinische Labordiagnostika AG

Laboratory diluter

• Primary Device ID: 04049016109754
• NIH Device Record Key: d0b87f3a-cfe9-44ac-b7e7-edf5da001e0f
• Commercial Distribution Discontinuation: 2020-02-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: EUROLabLiquidHandler (30-10)
• Version Model Number: YG 0830-0101-10
• 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	04049016109754 [Primary]

FDA Product Code

• JQW: Station, Pipetting And Diluting, For Clinical Use

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2020-02-17
• Device Publish Date: 2016-09-24

Devices Manufactured by EUROIMMUN Medizinische Labordiagnostika AG

• 04049016151876 - Sample buffer 2, Crithidia luciliae sensitive (IFA): 2025-03-14
• 04049016151890 - Sample buffer 2, Crithidia luciliae sensitive (IFA): 2025-03-14
• 04049016151920 - PBS-Tween (IFA): 2025-03-12
• 04049016151883 - Sample buffer (IFA): 2025-03-06
• 04049016151906 - Sample buffer (IFA): 2025-03-06
• 04049016151913 - Sample buffer (IFA): 2025-03-06
• 04049016151937 - PBS (IFA): 2025-03-06
• 04049016151944 - PBS (IFA): 2025-03-06