Primary Device ID | B29606107X400 |
NIH Device Record Key | 1da898e2-19d7-4055-b228-08d4ff9584a4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sonocath |
Version Model Number | 06-107X40 |
Company DUNS | 080306309 |
Company Name | TITUS MEDICAL LLC |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B29606107X400 [Primary] |
LKF | Cannula, Manipulator/Injector, Uterine |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-20 |
B29606107X400 | Case of 40 Units |
B29606107X10 | single unit |
B29606107X0 | box of 10 units |
B29606105X400 | Case of 40 Units |
B29606105X10 | single unit |
B29606105X0 | box of 10 units |
B2906105X30 | Case of 300 Units |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SONOCATH 85253863 4137679 Live/Registered |
Sterling Medical LLC 2011-02-28 |
SONOCATH 77875542 not registered Dead/Abandoned |
BOEZAART, ANDRE P. 2009-11-18 |