Adjustment solution

GUDID 04049016069355

EUROIMMUN Medizinische Labordiagnostika AG

Buffered wash solution IVD

• Primary Device ID: 04049016069355
• NIH Device Record Key: 35eb260f-4b7b-4dab-bbc4-ddb048de1c43
• Commercial Distribution Discontinuation: 2022-12-08
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Adjustment solution
• Version Model Number: ZE 1120-1050-6
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	04049016069355 [Primary]

FDA Product Code

• PPM: General Purpose Reagent

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: 2023-06-02
• Device Publish Date: 2022-12-08

On-Brand Devices [Adjustment solution]

• 04049016151821: ZE 1120-1850-7
• 04049016069355: ZE 1120-1050-6