Data-Cyte Plus 3% 213392

GUDID 07640137340278

Reagent Red Blood Cells panel used for identification of unexpected antibodies. For in vitro diagnostic use.

Medion Grifols Diagnostics AG

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• Primary Device ID: 07640137340278
• NIH Device Record Key: 072253c3-dcab-4fe6-bc84-5ffcfce53cef
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Data-Cyte Plus 3%
• Version Model Number: 11x4 ml
• Catalog Number: 213392
• Company DUNS: 483287020
• Company Name: Medion Grifols Diagnostics AG
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Device Kit: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07640137340278 [Primary]

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: 2018-03-29
• Device Publish Date: 2016-01-25

On-Brand Devices [Data-Cyte Plus 3%]

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