FDA.reportPublic FDA data

ProPatch-Kit

Primary DI
00185098000832
Brand
ProPatch-Kit
Company
PRO MEDICAL SUPPLIES, INC.
Model
ProM-013-Kit
Catalog number
ProM-013-Kit
Device description
Electrodes White Foam Back 1.5"x1.5" (1 pack with 4 electrodes) - Kit
Published
2016-08-24
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
false
OTC
true
Sterile
false
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
GXYElectrode, Cutaneous

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GXYElectrode, CutaneousNeurology2

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00185098000832PrimaryGS10
01850980008324Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00185098000832001850980008321850980008320185098000832
01850980008324018509800083241850980008324

GMDN Terms#

Term, Definition table
TermDefinition
Transcutaneous electrical stimulation electrodeA non-sterile electrical conductor intended to be attached to a patient's skin (noninvasive) to provide therapeutic electrical stimuli through the body surface [e.g., transcutaneous electrical nerve stimulation (TENS), electrical muscle stimulation, cranial electrotherapy stimulation (CES)]. It is typically a flat, flexible, conductive pad with an adhesive (e.g., gel), or a preformed shape/mechanism designed for attachment to a particular body part (e.g., earclip), connected to a conductive wire. This is a single-patient device that may be reapplied to the patient over a short term (single-use) before being discarded.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
215-938-0200sales@promedspecialties.com

Regulatory Flags#

DUNS number
135741127
Device count
4
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
false
Combination product
true
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
01085098000655PM-745PM-745PM-7452017-06-30
02085098000089ProPatchProM-033ProM-0332016-07-26
10185098000020ProM-200ProM-200ProM-2002016-08-24
10185098000037ProM-300ProM-300ProM-3002016-08-24
10185098000051ProM-500ProM-500ProM-5002016-08-24
10185098000068ProM-555ProM-555ProM-5552016-08-24
10185098000143ProPatchProM-036ProM-0362016-07-26
10185098000204ProPatchProM-021ProM-0212016-07-26
10185098000211ProPatchProM-032ProM-0322016-07-26
10185098000297PM-355PM-355PM-3552016-08-24
10185098000327PM-720PM-720PM-7202016-08-24
10185098000334ProPatchProM-024ProM-0242016-07-26
10185098000341Flex PlusProM-039ProM-0392016-07-26
10185098000372EcoPatchEco-020Eco-0202016-07-26
10185098000426EcoPatchEco-030Eco-0302016-07-26
10185098000433PM-360PM-360PM-3602016-08-24
10185098000440ProPatchProM-037ProM-0372016-07-26
10185098000631EcoPatchEco-021Eco-0212016-07-26
10185098000716StimPatchStim-021Stim-0212016-07-26
10185098000723StimPatchStim-020Stim-0202016-07-26

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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09342451004611Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02
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09342451004710Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02
09342451004727Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02
09342451004734Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02
09342451004741Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02
09342451004758Compumedics Quik-CapCOMPUMEDICS LIMITEDGXY2026-03-02