Primary Device ID | 08714729387947 |
NIH Device Record Key | 0b0b3b07-8607-440d-a5c2-c0739cc9dede |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Express²® |
Version Model Number | H7493507024220 |
Catalog Number | H7493507024220 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729387947 [Primary] |
MAF | STENT, CORONARY |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2014-09-24 |
08714729387954 | Coronary Stent System |
08714729387947 | Coronary Stent System |
08714729387879 | Coronary Stent System |
08714729387862 | Coronary Stent System |
08714729387794 | Coronary Stent System |
08714729387787 | Coronary Stent System |
08714729387718 | Coronary Stent System |
08714729387701 | Coronary Stent System |
08714729387657 | Coronary Stent System |
08714729387640 | Coronary Stent System |
08714729387060 | Coronary Stent System |
08714729387053 | Coronary Stent System |
08714729386988 | Coronary Stent System |
08714729386971 | Coronary Stent System |
08714729386902 | Coronary Stent System |
08714729386896 | Coronary Stent System |
08714729386827 | Coronary Stent System |
08714729386810 | Coronary Stent System |
08714729386766 | Coronary Stent System |
08714729386759 | Coronary Stent System |