FDA UDI In Commercial Distribution 🇺🇸 United States

SERIES-5 MyoVision FlexVision System

DI: 00853818007453 · Model: D2-D5 · PRECISION BIOMETRICS INC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SERIES-5 MyoVision FlexVision System
Primary DI
00853818007453
Version / Model
D2-D5
Catalog Number
D2-D5-D5
Company Name
PRECISION BIOMETRICS INC
Labeler DUNS
362997926
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-02-28
Public Version
1
Public Version Date
2021-03-08
Public Version Status
New
Public Device Record Key
d71c09e8-999d-4408-b3c4-087294c0f868

Device Description

SERIES-5 VisionHUB with FlexVision Inclinometers

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
KQX Goniometer, Ac-Powered
HCS Device, Temperature Measurement, Direct Contact, Powered
HCC Device, Biofeedback
IKN Electromyograph, Diagnostic

GMDN Terms

Code Name
32521 Multiple physiological signal amplifier

Identifiers

Type ID
Primary 00853818007453

Premarket Submissions

Submission Number Supplement Number
K123399 000