DAB Enhancer

GUDID 08435804512800

VITRO SA

Immunohistochemistry antibody detection IVD, reagent

• Primary Device ID: 08435804512800
• NIH Device Record Key: 189eec8b-dc1e-4ee2-8eb4-54c79fa19dcc
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DAB Enhancer
• Version Model Number: MAD-001560QVSBC
• Company DUNS: 466076718
• Company Name: VITRO SA
• 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	08435804512800 [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: 2025-02-28
• Device Publish Date: 2025-02-20

On-Brand Devices [DAB Enhancer]

• 08435804512800: MAD-001560QVSBC
• 08435421273047: MAD-001560QVS