Proteinase K (RTU)

GUDID 08435804522328

VITRO SA

Immunohistochemistry antibody detection IVD, reagent

• Primary Device ID: 08435804522328
• NIH Device Record Key: fbf91ef0-5ec4-4642-ba1f-dec0163133f7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Proteinase K (RTU)
• Version Model Number: MAD-011892QEVSBC
• 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	08435804522328 [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: 2025-08-18
• Device Publish Date: 2025-08-08

On-Brand Devices [Proteinase K (RTU)]

• 08435804522328: MAD-011892QEVSBC
• 08435804520713: MAD-011892QEVS