Primary Device ID | B040TF34 |
NIH Device Record Key | 3012a2a8-0863-4bf2-83d1-2f1d0b2ca6f4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | TransForm McCarthy Annuloplasty Ring |
Version Model Number | TF-34 |
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 | B040TF34 [Package] Contains: B040TF340 Package: [1 Units] In Commercial Distribution |
HIBCC | B040TF340 [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 | 2024-12-31 |
Device Publish Date | 2024-12-23 |
B040TF40 | Annuloplasty Ring |
B040TF38 | Annuloplasty Ring |
B040TF360 | Annuloplasty Ring |
B040TF34 | Annuloplasty Ring |
B040TF32 | Annuloplasty Ring |
B040TF30 | Annuloplasty Ring |
B040TF28 | Annuloplasty Ring |
B040TF26 | Annuloplasty Ring |
B040TF240 | Annuloplasty Ring |