Adjustment solution

GUDID 04049016069355

EUROIMMUN Medizinische Labordiagnostika AG

Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD Buffered wash solution IVD 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