Bio Protech

Primary DI
20817120020573
Brand
Bio Protech
Company
BIO PROTECH USA, INC.
Model
MaxIF 1k Unit
Device description
MaxIF 1k Unit- Interferential Analog Unit
Published
2016-09-01
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
LIHInterferential Current Therapy

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LIHInterferential Current TherapyNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K100246000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K100246000MAX-IF1000Bio Protech, Inc.2010-11-24LIH

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
10817120020576PackageGS15In Commercial Distribution
20817120020573PackageGS14In Commercial Distribution
00817120020579PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
1081712002057610817120020576
2081712002057320817120020573
00817120020579008171200205798171200205790817120020579

GMDN Terms#

Term, Definition table
TermDefinition
Interferential electrical stimulation systemAn electrically-powered device assembly designed to stimulate peripheral nerves through the transcutaneous application of two currents of slightly different frequencies (e.g., 4000 and 4100 Hz) that cross-over/interfere, producing a beating frequency (i.e., difference between the frequencies of both stimuli) at the treatment point. It typically consists of an external pulse generator and a set of electrodes placed in position to produce the interference at the desired point. The system is used mainly to relieve/manage intractable pain; some include additional electrodes to provide other types of electrical stimuli or suction for therapeutic massage.

Sterilization Methods#

Method table
Method

Contacts#

Phone, Email table
PhoneEmail
714-730-9950bioprotechusa@gmail.com

Regulatory Flags#

DUNS number
789127011
Device count
1
DM exempt
false
Premarket exempt
false
HCT/P
false
Kit
true
Combination product
false
Lot or batch
true
Serial number
true
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
00817120020050Bio Protech48482026-05-07
00817120020043Bio Protech48482016-06-15
00817120020340Bio Protech4848WCBZGN(NST)2016-06-21
00817120021088Bio ProtechSG15R (Lifelines)2017-08-09
00817120021095Bio ProtechSG15G (Lifelines)2017-08-09
00817120021101Bio ProtechNCS-1334 (Lifelines)2017-08-09
00817120021118Bio ProtechNCS-SG15 (Lifelines)2017-08-09
00817120021125Bio ProtechMF2409 (Lifelines)2017-08-09
00817120020005Bio Protech MaxTens 1k 2016-06-15
00817120020074Bio ProtechMaxEMS 1k2016-06-16
00817120020081Bio Protech MaxEMS 2k2016-06-17
00817120020562Bio Protech MaxTens 1k Unit2016-09-01
00817120020036Bio Protech MaxTens 2k 2016-06-16
00817120021132Bio ProtechDEEG-A-10 (Lifelines)2017-08-09
00817120021149Bio ProtechDEEG-A-12 (Lifelines)2017-08-09
00817120021156Bio ProtechDEEG-A-15 (Lifelines)2017-08-09
00817120021163Bio ProtechDEEG-A-20 (Lifelines)2017-08-09
00817120021170Bio ProtechRGEEG-05 (Lifelines)2017-08-09
00817120021187Bio ProtechRGEEG-10 (Lifelines)2017-08-09
00817120021194Bio ProtechRGEEG-12 (Lifelines)2017-08-09

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