PROEMG

Primary DI
08809083943431
Brand
PROEMG
Company
BIOPROTECH INC.
Model
BM3728
Device description
Monopolar Needle, Non-Wired, 37mmx0.36mm(D), Blue Hub
Published
2024-12-30
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Sterile
true
Single use
true

Product Codes#

Code, Name table
CodeName
GXZElectrode, Needle

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
GXZElectrode, NeedleNeurology2

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K152984000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K152984000Disposable Concentric Needle electrodes, Disposable Monopolar Needle electrodes, Disposable EP Needle electrodes, Disposable Hypodermic Needle electrodesBio Protech, Inc.2016-06-03IKT

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
18809083943438PackageGS125In Commercial Distribution
28809083943435PackageGS18In Commercial Distribution
08809083943431PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, EAN-13 table
Source identifierGTIN-14 normalizedEAN-13
1880908394343818809083943438
2880908394343528809083943435
08809083943431088090839434318809083943431

GMDN Terms#

Term, Definition table
TermDefinition
Electromyographic needle electrode, single-useA sterile electrical conducting device designed to be inserted percutaneously into muscle or nerve tissue to detect bioelectrical signal activity. It is a needle-like device (a needle electrode with an electrical connector at the proximal end) that is connected to an electromyograph (EMG) with a dedicated cable/lead. The EMG records the electrical signals and converts them into a readable graph format; it is not primarily intended for nerve stimulation. This is a single-use device.

Storage And Handling#

Type, Low, High table
TypeLowHighCondition
Storage Environment Humidity0 Degrees Celsius40 Degrees Celsius

Regulatory Flags#

DUNS number
688460539
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
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00851255007043Dynamic DIAGNOSTICS, INCPEN112025-03-12
00851255007098Dynamic DIAGNOSTICS, INCPEN312025-03-12
00851255007104Dynamic DIAGNOSTICS, INCPEN212025-03-12
00851255007111Dynamic DIAGNOSTICS, INCPEN412025-03-12
00851255007128Dynamic DIAGNOSTICS, INCP9551F2025-03-12
00851255007135Dynamic DIAGNOSTICS, INCP9552F2025-03-12
00851255007142Dynamic DIAGNOSTICS, INC9551F2025-03-12
00851255007159Dynamic DIAGNOSTICS, INC9552F2025-03-12
00851255007166Dynamic DIAGNOSTICS, INCP9551-RF2025-03-12
20851255007047Dynamic DIAGNOSTICS, INCPEN112025-03-12
00851255007050Dynamic DIAGNOSTICS, INCPEN11NS2025-03-12
00851255007067Dynamic DIAGNOSTICS, INCPEN31NS2025-03-12
00851255007074Dynamic DIAGNOSTICS, INCPEN21NS2025-03-12

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