PATHOS DELTA

GUDID 08052478980690

MILESTONE SRL

Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated Tissue processor IVD, automated/semi-automated

• Primary Device ID: 08052478980690
• NIH Device Record Key: 6dc732ac-f46b-4a77-8bcc-9f5736f0dc56
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PATHOS DELTA
• Version Model Number: 66000
• Company DUNS: 439086901
• Company Name: MILESTONE SRL
• 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: false
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08052478980690 [Primary]

FDA Product Code

• IEO: Processor, Tissue, Automated

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2022-09-16
• Device Publish Date: 2018-09-24