| Primary Device ID | 00879123007445 |
| NIH Device Record Key | 7c67a751-dd18-400a-aa86-80108410596b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BladderScan® |
| Version Model Number | i10™ |
| Catalog Number | 0570-0413 |
| 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 | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 | 00879123007445 [Primary] |
| ITX | Transducer, Ultrasonic, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-05-31 |
| Device Publish Date | 2021-05-21 |
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 |