Minncare HD 1% Indicator Test Strips

GUDID 30677964066895

MEDIVATORS INC.

Organic peroxy acid device sterilant, single-use

• Primary Device ID: 30677964066895
• NIH Device Record Key: 9c327972-2c9f-4d24-b2dc-7001cf4a92ce
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Minncare HD 1% Indicator Test Strips
• Version Model Number: 3029796
• Company DUNS: 068199363
• Company Name: MEDIVATORS INC.
• Device Count: 100
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00677964066894 [Unit of Use]
GS1	30677964066895 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K133724

FDA Product Code

• NIH: Disinfectant, Subsystem, Water Purification

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: 2018-03-29
• Device Publish Date: 2018-01-09

Devices Manufactured by MEDIVATORS INC.

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