Restore iProtect Module

Primary DI
00860190001498
Brand
Restore iProtect Module
Company
RESTORE MEDICAL SOLUTIONS, INC.
Model
R-1052-30-20
Device description
Instrument Module, 10 x 5 inch size
Published
2018-02-23
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

Product Codes#

Code, Name table
CodeName
KCTSterilization Wrap Containers, Trays, Cassettes & Other Accessories

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
KCTSterilization Wrap Containers, Trays, Cassettes & Other AccessoriesGeneral Hospital2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K131455000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K131455000RESTORE MODULAR STERILIZATION TRAY SYSTEMRestore Medical Solutions, Inc.2013-08-30KCT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00860190001498PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00860190001498008601900014988601900014980860190001498

GMDN Terms#

Term, Definition table
TermDefinition
Sterilization/disinfection containerA receptacle designed to hold wrapped and/or unwrapped medical devices in a chemical washer/disinfector and/or sterilizer during the washing/disinfection and/or sterilization cycle(s). It may be designed as a tray to allow full or partial immersion of the devices in a liquid disinfectant, or as an enclosed box to prevent contamination once the sterilization process is finished. The container may also be used for transport and storage of the processed devices, and may have features such as an expiry date label, breathing filter, built-in slots for microsurgical instruments, and stacking capabilities. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
032044173
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00860190001405Restore Intelligent Sterilization TrayR-10204-002018-02-23
00860190001412Restore Advanced Stringer SystemR-STR-A102018-02-23
00860190001429Restore Advanced Stringer SystemR-STR-A92018-02-23
00860190001436Restore IQ SystemR-A1010-FR2-402018-02-23
00860190001443Restore IQ SystemR-A1016-FR2-402018-02-23
00860190001450Restore IQ SystemR-A1020-FR2-402018-02-23
00860190001467Restore IQ SystemR-1010-FR2-102018-02-23
00860190001474Restore IQ SystemR-1016-FR2-102018-02-23
00860190001481Restore IQ SystemR-1020-FR2-102018-02-23

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