Primary Device ID | 04961333244133 |
NIH Device Record Key | c8cad243-b132-4e07-a423-82273e652518 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NOBLUS |
Version Model Number | NOBLUS |
Company DUNS | 083211284 |
Company Name | PENTAX OF AMERICA, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04961333244133 [Primary] |
IYN | System, Imaging, Pulsed Doppler, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2018-03-15 |
04961333244157 | HITACHI NOBLUS UTRASND PROC |
04961333244140 | NOBLUS DEMO CRATE |
04961333244133 | HITACHI NOBLUS UTRASND PROC W/ SONOELAST |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() NOBLUS 85547876 4397013 Live/Registered |
KABUSHIKI KAISHA HITACHI SEISAKUSHO 2012-02-21 |