InflammaDry RPS-ID-20

GUDID 30014613336747

InflammaDry

QUIDEL CORPORATION

Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical Matrix metalloproteinase-9 (MMP-9) IVD, kit, rapid ICT, clinical

• Primary Device ID: 30014613336747
• NIH Device Record Key: b0e61b13-929c-4eef-8237-9731fc3eb3ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: InflammaDry
• Version Model Number: RPS-ID-20
• Catalog Number: RPS-ID-20
• Company DUNS: 079509836
• Company Name: QUIDEL CORPORATION
• Device Count: 1
• DM Exempt: false
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com
• Phone: +1(858)552-1100
• Email: technicalsupport@quidel.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	30014613336747 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K132066

FDA Product Code

• PFQ: MMP-9 test system

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: 2023-06-16
• Device Publish Date: 2019-08-02

On-Brand Devices [InflammaDry]

• 30014613336754: InflammaDry
• 30014613336747: InflammaDry