EUROLabLiquidHandler (30-08)

GUDID 04049016109778

EUROIMMUN Medizinische Labordiagnostika AG

Laboratory diluter

• Primary Device ID: 04049016109778
• NIH Device Record Key: de7572e4-6203-441f-9ae5-944845f07ea2
• Commercial Distribution Discontinuation: 2020-02-14
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: EUROLabLiquidHandler (30-08)
• Version Model Number: YG 0830-0101-8
• 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	04049016109778 [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

• 04049016152057 - EUROArray wash buffer set: 2026-02-04
• 04049016151814 - ELISA wash buffer 10x conc.: 2026-01-21
• 04049016116110 - Anti-Echinococcus EUROLINE WB (IgG): 2026-01-19
• 04049016151951 - Tween 20 (IFA): 2026-01-14
• 04049016151968 - Tween 20 (IFA): 2026-01-14
• 04049016092599 - Anti-Glutamate receptor (type NMDA) IFA: 2025-12-29
• 04049016092605 - Anti-Glutamate receptor (type NMDA) IFA: 2025-12-29
• 04049016126034 - EUROArrayScan: 2025-12-29