Restore iProtect Module

GUDID 00860190001498

Instrument Module, 10 x 5 inch size

RESTORE MEDICAL SOLUTIONS, INC.

Sterilization/disinfection container Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable Device sterilization/disinfection container, reusable

• Primary Device ID: 00860190001498
• NIH Device Record Key: 417070d2-fe8a-40d0-9748-cdc9a676caf5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Restore iProtect Module
• Version Model Number: R-1052-30-20
• Company DUNS: 032044173
• Company Name: RESTORE MEDICAL SOLUTIONS, INC.
• 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: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: true
• Serial Number: false
• 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	00860190001498 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K131455

FDA Product Code

• KCT: Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

Sterilization

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

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

[00860190001498]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-09-10
• Device Publish Date: 2018-02-23

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