Primary Device ID | 10879123004595 |
NIH Device Record Key | 8acd6a31-6f59-4537-8f46-998af04c0498 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BladderScan® |
Version Model Number | Prime |
Catalog Number | 0800-0532 |
Company DUNS | 130598584 |
Company Name | VERATHON 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 | true |
Serial Number | false |
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 | 00879123004598 [Primary] |
GS1 | 10879123004595 [Package] Contains: 00879123004598 Package: [1 Units] In Commercial Distribution |
IYO | System, Imaging, Pulsed Echo, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BLADDERSCAN 78174469 2829901 Live/Registered |
VERATHON INC. 2002-10-15 |
BLADDERSCAN 74216827 not registered Dead/Abandoned |
Diagnostic Ultrasound Corporation 1991-10-29 |
BLADDERSCAN 73793955 not registered Dead/Abandoned |
DIAGNOSTIC ULTRASOUND CORPORATION 1989-04-17 |