Primary Device ID | B040FRN28 |
NIH Device Record Key | 62878493-53be-4025-a34d-8c9658d669ae |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlexForm Annuloplasty Ring |
Version Model Number | FRN-28 |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B040FRN28 [Package] Contains: B040FRN2802 Package: [1 Units] In Commercial Distribution |
HIBCC | B040FRN2802 [Primary] |
KRH | Ring, Annuloplasty |
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 | 2017-02-01 |
B040FRN40 | Annuloplasty Ring |
B040FRN38 | Annuloplasty Ring |
B040FRN36 | Annuloplasty Ring |
B0040FRN34 | Annuloplasty Ring |
B040FRN32 | Annuloplasty Ring |
B040FRN30 | Annuloplasty Ring |
B040FRN28 | Annuloplasty Ring |
B040FRN26 | Annuloplasty Ring |
B040FRN240 | Annuloplasty Ring |
B040FRH40 | Annuloplasty Ring |
B040FRH38 | Annuloplasty Ring |
B040FRH36 | Annuloplasty Ring |
B040FRH34 | Annuloplasty Ring |
B040FRH32 | Annuloplasty Ring |
B040FRH30 | Annuloplasty Ring |
B040FRH28 | Annuloplasty Ring |
B040FRH26 | Annuloplasty Ring |
B040FRH24 | Annuloplasty Ring |