CureWrap™

Primary DI
07290012127335
Brand
CureWrap™
Company
M.T.R.E. ADVANCED TECHNOLOGIES LTD.
Model
Pediatric, 79-91cm (single)
Catalog number
500-03531
Device description
Accessory for the CritiCool system. A body wrap connected to the CritiCool.
Published
2016-09-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
DWJSystem, Thermal Regulating

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DWJSystem, Thermal RegulatingCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
17290012127332PackageGS18In Commercial Distribution
77290012127334PackageGS14In Commercial Distribution
07290012127335PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1729001212733217290012127332
7729001212733477290012127334
07290012127335072900121273357290012127335

GMDN Terms#

Term, Definition table
TermDefinition
Circulating-fluid whole-body heating/cooling system control unitA mains electricity (AC-powered) device intended to be used as part of a circulating-fluid whole-body heating/cooling system to control/regulate the temperature and flow of fluid through a connected patient-applied pad (not included), for heating and alternatively cooling a patient’s whole-body (i.e., elevate or lower core body temperature). The device includes a heater and refrigeration unit, a pump, and typically a water reservoir; it may also be intended for patient temperature monitoring and typically includes alarms for cases of water temperatures beyond pre-set limits. It is intended to be used by a healthcare professional in a clinical setting (e.g., to achieve normothermia).

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
+2152591020info@mmi.co.il

Regulatory Flags#

DUNS number
532022530
Device count
1
DM exempt
false
Premarket exempt
true
HCT/P
false
Kit
false
Combination product
false
Lot or batch
true
Serial number
false
Manufacturing date on label
false
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
false
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
07290107580526CritiCool Pro VL4000N 115VAC100-000132016-09-24
07290107580540CritiCool Pro VL4000M 115VAC100-001132016-09-24
07290107580564CritiCool Pro VL4500N 115VAC100-002132016-09-24
07290107580588CritiCool Pro VL4500M 115VAC100-003132016-09-26
07290102932313CritiCool ProVitaLogik4000 3/5Lead,NI Nellcor Blue681-0R0-0132016-09-24
07290102932337CritiCool ProVitaLogik4000 3/5Lead,NI Masimo Blue681-0R0-0232016-09-24
07290102932344CritiCool ProVitaLogik4500 3/5Lead Nellcor Blue681-0R0-1132016-09-24
07290102932351CritiCool ProVitaLogik4500 3/5Lead Masimo Blue681-0R0-1232016-09-24
07290102932368CerebralogikModule CC Set Color681-138-0002016-09-24
07290102932375Cerebralogik Module VL Set Color681-138-0102016-09-24
07290102932382Cerebralogik aEEG VL4X00_Kit 681-OPT-1382016-09-24
07290102932399Cerebralogik aEEG VL6X00_Kit781OPT1382016-09-24
77290107580242CureWrap™X-Large Pediatric 122-135 cm (single)PED-X10012016-09-24
77290107580266CureWrap™X-Large Pediatric over 135cm (single)PED-X20012016-09-24

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