PRODESSE 303677

GUDID 15420045506398

Hologic, Inc.

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• Primary Device ID: 15420045506398
• NIH Device Record Key: 4c8c2d9d-c2fa-4a89-99a6-ddf88dfe368c
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: PRODESSE
• Version Model Number: PROPARAFLU+ KIT, 100 REACTIONS
• Catalog Number: 303677
• Company DUNS: 050579217
• Company Name: Hologic, Inc.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• 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	15420045506398 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132238

FDA Product Code

• OOU: Parainfluenza multiplex nucleic acid assay

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-04-15

On-Brand Devices [PRODESSE]

• 15420045506398: PROPARAFLU+ KIT, 100 REACTIONS
• 15420045506381: PROADENO+ KIT, 100 REACTIONS
• 15420045506374: PROFAST+ KIT, 100 REACTIONS
• 15420045506367: PRO HMPV+ KIT, 100 REACTIONS
• 15420045506350: PROGASTRO SSCS ASSAY
• 15420045506343: PROFLU+ ASSAY KIT, 1,500 REACTIONS
• 15420045506336: PROFLU+ ASSAY KIT, 2,000 REACTIONS
• 15420045506329: PRODESSE PROFLU+ ASSAY