Minncare HD Residual Test Strips

GUDID 30677964066888

MEDIVATORS INC.

Organic peroxy acid device sterilant, single-use

• Primary Device ID: 30677964066888
• NIH Device Record Key: c9a0a847-e2ac-4436-bb66-2c1f76830e7a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Minncare HD Residual Test Strips
• Version Model Number: 3029795
• 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	00677964066887 [Unit of Use]
GS1	30677964066888 [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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• 40677964050037 - Endo Carry-on Procedure Kit: 2024-08-15 Endo Carry-on Procedure Kit Includes Basin, Intercept Detergent, Cylindrical Sponge, Absorbent Pad, Lubricant and Gauze.
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