VENTANA HE 600 Coverslip Activator 07534396001

GUDID 04015630967117

Ventana Medical Systems, Inc.

Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Programmed death-ligand 1 (PD-L1) IVD, antibody Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD Xylene solution substitute IVD

• Primary Device ID: 04015630967117
• NIH Device Record Key: 05aa31e3-c4ce-43e9-b3cd-db555c058d08
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VENTANA HE 600 Coverslip Activator
• Version Model Number: 07534396001
• Catalog Number: 07534396001
• Company DUNS: 184042521
• Company Name: Ventana Medical Systems, Inc.
• 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: true
• Serial Number: false
• Manufacturing Date: false
• 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	04015630967117 [Primary]

FDA Product Code

• PPM: General purpose reagent

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-11
• Device Publish Date: 2021-02-03

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