VERMED

Primary DI
35060441915420
Brand
VERMED
Company
NISSHA MEDICAL TECHNOLOGIES LTD
Model
F7956P
Catalog number
4011015C
Device description
Disposable multifunctionelectrodes for defibrillation, synchronized cardioversion, transcutaneous cardiac stimulation and ECG monitoring, with direct connection to cables and defibrillators
Published
2018-01-08
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

Product Codes#

Code, Name table
CodeName
LDDDc-Defibrillator, Low-Energy, (Including Paddles)

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LDDDc-Defibrillator, Low-Energy, (Including Paddles)Cardiovascular2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K103783000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K103783000EURO DEFI PADS ADULT; EURO DEFI PADS ADULT RADIOTRANSPARENT: EURO DEFI PADS PEDIATRICFiab Spa2011-06-16LDD

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
35060441915420PackageGS15In Commercial Distribution
15060441915426PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized table
Source identifierGTIN-14 normalized
3506044191542035060441915420
1506044191542615060441915426

GMDN Terms#

Term, Definition table
TermDefinition
External defibrillator electrode padA conductive medium designed to be used between the metal contact surface of an external defibrillator electrode, of the paddle-type, and the patient's skin. A defibrillator electrode pad is available in two basic designs: 1) a thickened conductive gel or polymer layer reinforced by a non-woven material; or 2) a conductive adhesive pad with a metal contact on its outer surface. This is a single-use device.

Sterilization Methods#

Method table
Method

Regulatory Flags#

DUNS number
671405566
Device count
1
DM exempt
false
Premarket exempt
false
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
true
Sterilization required before use
false

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
15060441917826swaromed10366000045C2026-04-07
15060441918212swaromed40366000578C2026-04-07
15060441918229swaromed40666000581C2026-04-07
15060441918236swaromed40096000582C2026-04-07
15060441918250swaromed40606000588C2026-04-07
15060441918755swaromed40406001237C2026-04-07
15060842920197N/AGX1-1285H2025-06-18
15060842920210N/AGX1-1280H2025-06-18
35060842920191N/AGX1-1285H2025-06-18
35060842920214N/AGX1-1280H2025-06-18
15060842920234Corpuls1019CO19101.192025-02-18
35060842920238Corpuls1019CO19101.192025-02-18
15060842920142DrägerFW50DR7000018722024-03-01
15060842920159DrägerFW32PDR7000018732024-03-01
35060842920146DrägerFW50DR7000018722024-03-01
35060842920153DrägerFW32PDR7000018732024-03-01
15060441915105VERMEDF7957W4011003C2018-01-11
15060441915174VERMEDF79504010989C2018-01-08
15060441915181VERMEDF79514010990C2018-01-08
15060441915198VERMEDF79524010991C2018-01-08

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