GoWISE USA

Primary DI
20819687020119
Brand
GoWISE USA
Company
MING'S MARK INC.
Model
GW22063
Published
2017-07-26
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
MR Safe
Rx
false
OTC
false
Sterile
false
Single use
false

Product Codes#

Code, Name table
CodeName
OFECentral Venous Blood Pressure Kit

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
OFECentral Venous Blood Pressure KitCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10819687020112PackageGS11In Commercial Distribution
20819687020119PackageGS118In Commercial Distribution
00819687020115PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081968702011210819687020112
2081968702011920819687020119
00819687020115008196870201158196870201150819687020115

GMDN Terms#

Term, Definition table
TermDefinition
Physiologic-monitoring defibrillation systemAn assembly of electrically-powered devices designed to defibrillate the heart that incorporates additional therapeutic and/or monitoring features intended to resuscitate and/or monitor a cardiac patient. It typically includes devices that enable manual and/or automated external defibrillation (a defibrillator) and one or more of the following: electrocardiogram (ECG) monitoring (electrocardiograph), noninvasive cardiac pacing (temporary pacemaker), cardioversion (CV), pulse oximetry (oximeter), invasive and/or noninvasive blood pressure monitoring, and end-tidal carbon dioxide (EtCO2) monitoring (i.e., a CO2 monitor). It may have data recording/printing capabilities.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
005175432
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
false
Lot or batch
false
Serial number
true
Manufacturing date on label
true
Expiration date on label
false
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
00853821006030GoWISE USAGW220292016-08-23
00819687020115GoWISE USA GW220632017-07-26
00819687020290GoWISE USA GW220412017-12-29
00819687020306GoWISE USA GW220422017-12-29
00853113007028GoWISE USA GW220512016-12-06
00853821006368GoWISE USA GW220402017-03-12
20853113007022GoWISE USA GW220512016-12-06
00853821006023GoWISE USAGW220252016-08-23
00853821006047GoWISE USAGW220272016-08-23
20853821006362GoWISE USA GW220402017-03-12
00853821006825GoWISE USAGW220612016-08-23
20819687020294GoWISE USA GW220412017-12-29
20819687020300GoWISE USA GW220422017-12-29

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
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50197106547395CARDINAL HEALTHCardinal Health 200, LLCOFE2024-01-29