SWAROMED

Primary DI
39120026223596
Brand
SWAROMED
Company
TYROLMED GmbH
Model
4008
Catalog number
6001473N
Device description
ECG Electrodes
Published
2019-05-03
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
OTC
false
Sterile
false
Single use
true

Product Codes#

Code, Name table
CodeName
DRXElectrode, Electrocardiograph

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
DRXElectrode, ElectrocardiographCardiovascular2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
29120026223599PackageGS18In Commercial Distribution
39120026223596PackageGS112In Commercial Distribution
19120026223592PrimaryGS10
09120026223595Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
2912002622359929120026223599
3912002622359639120026223596
1912002622359219120026223592
09120026223595091200262235959120026223595

GMDN Terms#

Term, Definition table
TermDefinition
Electrocardiographic electrode, single-useA non-sterile, noninvasive electrical conductor designed to conduct electrical signals, generated by a patient's heart, from the skin surface to an electrocardiograph (ECG) monitoring device, via an ECG lead wire (not included). It is typically a disk-like electrode that is affixed to the skin with a special adhesive, adhesive tape, or suction mechanism; a conductive gel may be pre-applied and it may include a skin cleaning wipe to assist electrical connection. Electrocardiography is usually performed using a set of electrodes (e.g., 10) connected to appropriate leads and cables. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Temperature0 Degrees Celsius40 Degrees Celsius

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
300387502
Device count
50
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
true
Expiration date on label
true
Donation ID number
false
Contains natural rubber latex
false
No natural rubber latex
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
19120026223509SWAROMED1036FT6000407N2019-05-03
19120026223523SWAROMED40776001317N2019-05-03
19120026223547SWAROMED40516001418N2019-05-03
19120026223592SWAROMED40086001473N2019-05-03
19120026223677SWAROMED40026001446N2019-05-03
19120026223684SWAROMED40506001479N2019-05-03
19120026223707SWAROMED41026001484N2019-05-03
19120026223714SWAROMED41116001486N2019-05-03
19120026223721SWAROMED41126001487N2019-05-03
19120026223738SWAROMED10856001481N2019-05-03
19120026223745SWAROMED17026001482N2019-05-03
19120026223752SWAROMED40236001483N2019-05-03
19120026223776SWAROMED47016001488N2019-05-03
19120026223783SWAROMED47036001489N2019-05-03
19120026223790SWAROMED47046001490N2019-05-03
39120026223503SWAROMED1036FT6000407N2019-05-03
39120026223527SWAROMED40776001317N2019-05-03
39120026223541SWAROMED40516001418N2019-05-03
39120026223671SWAROMED40026001446N2019-05-03
39120026223688SWAROMED40506001479N2019-05-03

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Primary DI, Brand, Company table
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08809083949136TELECTRODEBIOPROTECH INC.DRX2026-04-30
20192253017080KendallCardinal Health 200, LLCDRX2023-03-16
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