ASSY,Reag.Disp.Card,PrepKit 82,BenchMark 05254035001

GUDID 07613336125991

Ventana Medical Systems, Inc.

Assay container IVD, single-use

• Primary Device ID: 07613336125991
• NIH Device Record Key: 53f8a70a-8520-4dc9-bf4b-3368e693ff57
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASSY,Reag.Disp.Card,PrepKit 82,BenchMark
• Version Model Number: 05254035001
• Catalog Number: 05254035001
• 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: true
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07613336125991 [Primary]

FDA Product Code

• JRC: MICRO PIPETTE

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: 2025-07-15
• Device Publish Date: 2025-07-07

On-Brand Devices [ASSY,Reag.Disp.Card,PrepKit 82,BenchMark]

• 07613336127551: 05252237001
• 07613336125991: 05254035001