Primary Device ID | B296061070 |
NIH Device Record Key | 652f5a66-ccdc-46fe-932f-1397ad754f11 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HSG Catheter |
Version Model Number | 06-107 |
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 | B296061070 [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 | 2016-09-16 |
B296E07070 | single unit |
B296E0700FR03 | single unit |
B296E0700FIRM00 | single unit |
B296E050507 | single unit |
B296E0500FR01 | single unit |
B296E0500FIRM0 | single unit |
B296C070709 | Case of 40 Units |
B296C0700FR01 | Case of 40 Units |
B296C0700FIRM0 | Case of 40 Units |
B296C050505 | Case of 40 Units |
B296C0500FR0 | Case of 40 Units |
B296C0500FIRM0 | Case of 40 Units |
B296B070708 | box of 10 units |
B296B0700FR00 | box of 10 units |
B296B0700FIRM0 | box of 10 units |
B296B05050 | box of 10 units |
B296B0500FR0 | box of 10 units |
B296B0500FIRM0 | box of 10 units |
B29606107F400 | Case of 40 Units |
B29606107F10 | single unit |
B29606107F0 | box of 10 units |
B296061070 | Case of 100 Units Bulk |
B29606105F400 | Case of 40 Units |
B29606105F10 | single unit |
B29606105F0 | box of 10 units |
B296061050 | Case of 100 Units Bulk |