EUROLabWorkstation IFA

GUDID 04049016137986

EUROIMMUN Medizinische Labordiagnostika AG

Multichannel immunoassay analyser IVD

• Primary Device ID: 04049016137986
• NIH Device Record Key: d6c78be6-5641-4a82-afdf-321304fb49ea
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: EUROLabWorkstation IFA
• Version Model Number: YG 0852-0101
• 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	04049016137986 [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: 2
• Public Version Date: 2025-06-30
• Device Publish Date: 2022-12-08

Devices Manufactured by EUROIMMUN Medizinische Labordiagnostika AG

• 04049016137986 - EUROLabWorkstation IFA: 2025-06-30
• 04049016137986 - EUROLabWorkstation IFA: 2025-06-30
• 04049016140368 - Dehydroepiandrosterone Sulfate (DHEA-S) ELISA: 2025-06-30
• 04049016147602 - Free Estriol ELISA: 2025-06-30
• 04049016152088 - TITERPLANE set for the incubation of slides with 50 fields: 2025-06-10
• 04049016152040 - WASH REAGENT 2: 2025-05-21
• 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