Primary Device ID | 20650862199073 |
NIH Device Record Key | 9db1d50b-fdae-4c23-b4c7-0cdb72c193a3 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | 19907 |
Company DUNS | 051798999 |
Company Name | ATRIUM MEDICAL CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00650862199079 [Primary] |
GS1 | 20650862199073 [Package] Contains: 00650862199079 Package: [10 Units] In Commercial Distribution |
KDQ | BOTTLE, COLLECTION, VACUUM |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-01-15 |
Device Publish Date | 2015-09-24 |
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00650862425383 - iCast Covered Stent System, 5mmX38mmX120cm | 2023-06-19 iCast Covered Stent System, 5mmX38mmX120cm |
00650862425598 - iCast Covered Stent System, 5mmX59mmX120cm | 2023-06-19 iCast Covered Stent System, 5mmX59mmX120cm |
00650862426168 - iCast Covered Stent System, 6mmX16mmX120cm | 2023-06-19 iCast Covered Stent System, 6mmX16mmX120cm |
00650862426229 - iCast Covered Stent System, 6mmX22mmX120cm | 2023-06-19 iCast Covered Stent System, 6mmX22mmX120cm |
00650862426380 - iCast Covered Stent System, 6mmX38mmX120cm | 2023-06-19 iCast Covered Stent System, 6mmX38mmX120cm |