PROTEASE 1 05266688001

GUDID 04015630971138

Ventana Medical Systems, Inc.

Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Negative control immunoglobulin IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD Immunohistochemistry protease reagent IVD

• Primary Device ID: 04015630971138
• NIH Device Record Key: 65d14a22-f3c9-4781-9dfe-426efaab0e43
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PROTEASE 1
• Version Model Number: 05266688001
• Catalog Number: 05266688001
• 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	04015630971138 [Primary]

FDA Product Code

• IBG: TRYPSIN

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: 2021-02-08
• Device Publish Date: 2021-01-29

Devices Manufactured by Ventana Medical Systems, Inc.

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• 04015630970063 - CONFIRM anti-ALK1 (ALK01) Primary Antibody: 2022-12-15
• 04015630970445 - CINtec® p16 Histology: 2022-12-15
• 04015630971015 - Anti-p53 (Bp53-11) Primary Antibody: 2022-12-15
• 04015630971053 - CONFIRM anti-Cytokeratin 20 (SP33) Rabbit Monoclonal Primary Antibody: 2022-12-15
• 04015630971183 - CONFIRM anti-CD15 (MMA) Mouse Monoclonal Primary Antibody: 2022-12-15