ASSY,Reag.Disp.Card,PrepKit 72,BenchMark 05253918001

GUDID 07613336125892

Ventana Medical Systems, Inc.

Assay container IVD, single-use

• Primary Device ID: 07613336125892
• NIH Device Record Key: 5f5b93ff-4239-4b2e-bf3b-620f8fa1681c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ASSY,Reag.Disp.Card,PrepKit 72,BenchMark
• Version Model Number: 05253918001
• Catalog Number: 05253918001
• 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	07613336125892 [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 72,BenchMark]

• 07613336127452: 05252113001
• 07613336125892: 05253918001