FDA UDI In Commercial Distribution 🇺🇸 United States

BioEMG

DI: 00860003499900 · Model: III NRG V2 · Bio-Research Associates, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
BioEMG
Primary DI
00860003499900
Version / Model
III NRG V2
Company Name
Bio-Research Associates, Inc.
Labeler DUNS
063501373
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-06-22
Public Version
1
Public Version Date
2023-06-30
Public Version Status
New
Public Device Record Key
0d6a683f-add5-47a3-866b-945c1231a140

Device Description

Indications for use: 8 channel EMG Amplifier 1. To record electrical activity of muscles of the stomatognathic system, especially temporalis, masseter and digastric. 2. To clinically monitor up to eight different muscles as an aid in the diagnosis and treatments evaluation by recording the electrical activity of muscles of the stomatognathic system. 3. To determine the degree of relaxation (intra-patient) of a single muscle/group of muscles at rest. 4. To measure relative (intra-patient) levels of activity of several muscles during a functional act. Indications for use: 2 channel JVA amplifier 1. To record and display sounds/vibrations from the temporomandibular joints. 2. To aid the clinician in their analysis of a joint sound/vibration by allowing them to see the waveform in various standard plots. 3. To aid the clinician in comparing a patient's current stand plots to previous recordings before, during, and after treatment. 4. To provide numerical values that can be used to quantify the physical characteristics of the sounds/vibrations, allowing intra-patient comparisons (only) by the clinician.

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KZM Device, Muscle Monitoring

GMDN Terms

Code Name
47556 Jaw physiology evaluation system

Identifiers

Type ID
Primary 00860003499900

Customer Contacts

Phone
4143577525

Premarket Submissions

Submission Number Supplement Number
K082927 000