Primary Device ID | B040TRH30 |
NIH Device Record Key | 6a192d75-8dc5-44f3-9795-f9d644ef4ad9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TruForm Annuloplasty Ring |
Version Model Number | TRH-30 |
Company DUNS | 939872651 |
Company Name | GENESEE BIOMEDICAL, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com | |
Phone | 800 786-4890 |
info@geneseebiomedical.com |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B040TRH30 [Package] Contains: B040TRH300 Package: [1 Units] In Commercial Distribution |
HIBCC | B040TRH300 [Primary] |
KRH | Ring, Annuloplasty |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-12-12 |
Device Publish Date | 2024-12-04 |
B040TRH42 | Annuloplasty Ri |
B040TRH40 | Annuloplasty Ri |
B040TRH38 | Annuloplasty Ri |
B040TRH36 | Annuloplasty Ri |
B040TRH34 | Annuloplasty Ri |
B040TRH32 | Annuloplasty Ri |
B040TRH30 | Annuloplasty Ring |
B040TRH28 | Annuloplasty Ring |
B040TFH26 | Annuloplasty Ring |
B040TRH24 | Annuloplasty Ring |