FDA.reportPublic FDA data

Biowave Percutaneous Electrodes

Primary DI
00859911006027
Brand
Biowave Percutaneous Electrodes
Company
BIOWAVE CORPORATION
Model
MK78515 - BWEP02-E
Device description
Biowave Percutaneous Electrode Set - E
Published
2016-08-01
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
NHIStimulator, Nerve, Electrial, Percutaneous (Pens), For Pain Relief

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
NHIStimulator, Nerve, Electrical, Percutaneous (Pens), For Pain ReliefNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K061166000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K061166000DEEPWAVE PERCUTANEOUS NEUROMODULATION PAIN THERAPY SYSTEMBiowave Corporation2006-08-15NHI

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10859911006024PackageGS16In Commercial Distribution
20859911006021PackageGS172In Commercial Distribution
00859911006027PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1085991100602410859911006024
2085991100602120859911006021
00859911006027008599110060278599110060270859911006027

GMDN Terms#

Term, Definition table
TermDefinition
Analgesic PENS system probe, single-useA sterile, hand-held electrical conductor intended to be used as part of an analgesic percutaneous electrical nerve stimulation (PENS) system to deliver controlled electrical impulses directly to subcutaneous tissue for the relief of chronic neuropathic pain. It is intended to be connected to an analgesic PENS system generator and its conductive length introduced percutaneously (invasively) into the patient, in the vicinity of a peripheral nerve. This is a single-use device.

Storage And Handling#

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

Contacts#

Phone, Email table
PhoneEmail
1-877-246-9283info@biowave.com

Regulatory Flags#

DUNS number
005759084
Device count
1
Lot or batch
true
Manufacturing date on label
true
Expiration date on label
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00859911006140BioWave Noninvasive ElectrodesGOPADS_12023-08-07
00859911006232BioWave Silver Back BioWrap S/MBWRPSILVER-BACK-SM2023-08-07
00859911006249BioWave Silver Knee BioWrap S/MBWRPSILVER-KNEE-SM2023-08-07
00859911006256BioWave Silver Foot-Ankle BioWrap S/MBWRPSILVER-FOOT-ANKLE-SM2023-08-07
00859911006461BioWave Silver Back BioWrap L/XLBWRPSILVER-BACK-LXL2023-08-07
00859911006492BioWave Silver Foot-Ankle BioWrap L/XLBWRPSILVER-FOOT-ANKLE-LXL2023-08-07
00859911006508BioWave Silver Knee BioWrap L/XLBWRPSILVER-KNEE-LXL2023-08-07
00859911006546BioWave Silver Thigh-Calf BioWrap S/MBWRPSILVER-THIGH-CALF-SM2023-08-07
00859911006560BioWave Silver Thigh-Calf BioWrap L/XLBWRPSILVER-THIGH-CALF-LXL2023-08-07
00859911006577BioWave BLUE Back BioWrap L/XLBWRPBLUE-BACK-LXL2023-08-07
00859911006584BioWave BLUE Back BioWrap S/MBWRPBLUE-BACK-SM2023-08-07
00859911006591BioWave BLUE Knee BioWrap L/XLBWRPBLUE-KNEE-LXL2023-08-07
00859911006607BioWave Noninvasive Velcro Backed Electrodes - B-SetBIOWRAP-PADS2023-08-07
00859911006669BioWave BLUE Knee BioWrap S/MBWRPBLUE-KNEE-SM2023-08-07
00859911006065BiowavePROBWPD012016-08-01
00859911006430BioWaveGO RXBWG-RX2023-06-15
00859911006010BioWaveGOBWG-S2021-07-26
00859911006072BiowaveHOMEBWHD012016-08-01
00859911006089Biowave Noninvasive ElectrodesMK78560 - BWEN01-B2016-08-01
00859911006096Biowave Noninvasive ElectrodesMK78570 - BWEN02-E2016-08-01

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
08908006064328POSP DeviceNEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2026-05-22
00850022775260SPRINTSPR THERAPEUTICS, INC.NHI2026-05-19
08908006064199Primary Relief NEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2026-03-16
08908006064212NociRelief NEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2026-03-16
08908006064236NS100NEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2026-03-16
08908006064267ANSiSTIM - PP NEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2026-03-16
00850022775000SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775017SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775222SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775239SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775246SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775253SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775376SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775383SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775444SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775451SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775468SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775475SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775482SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775499SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775505SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775512SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775529SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775536SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775543SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775550SPRINTSPR THERAPEUTICS, INC.NHI2026-01-06
00850022775413SPRINTSPR THERAPEUTICS, INC.NHI2025-08-21
08908006064250NEUMONANEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2025-08-18
08908006064168POSP Device NEUROSTIMULATION MEDTECH PRIVATE LIMITEDNHI2025-05-19
00850022775390SPRINTSPR THERAPEUTICS, INC.NHI2024-08-30