Primary Device ID | 15420045505957 |
NIH Device Record Key | e9a1e5b2-8870-4575-b485-5df1ee598b71 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Selenia FFDM |
Version Model Number | ASY-01366 |
Catalog Number | ASY-01366 |
Company DUNS | 139534114 |
Company Name | Hologic, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 15420045505957 [Primary] |
MUE | Full field digital,system,x-ray,mammographic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-03-30 |
15420045507920 | 4-000-0308 |
15420045507913 | ASY-05468 |
15420045507890 | 4-000-0144 |
15420045507883 | 3-000-4617 |
15420045507876 | 3-000-1528 |
15420045507715 | FAB-00752 |
15420045507708 | FAB-00609 |
15420045507692 | 4-000-0293 |
15420045507685 | 3-535-0087 |
15420045507678 | 3-535-0012 |
15420045507586 | FAB-00754 |
15420045507579 | FAB-00610 |
15420045507562 | FAB-00608 |
15420045507555 | 5-000-0073 |
15420045507548 | 5-000-0072 |
15420045506060 | ASY-07973 |
15420045506053 | ASY-06758 |
15420045506046 | ASY-06755 |
15420045506039 | ASY-06754 |
15420045506022 | ASY-06753 |
15420045506015 | ASY-06717 |
15420045506008 | ASY-06716 |
15420045505995 | ASY-06715 |
15420045505988 | ASY-06714 |
15420045505971 | ASY-01656 |
15420045505964 | ASY-01427 |
15420045505957 | ASY-01366 |
15420045505940 | ASY-00676 |
15420045505933 | ASY-00834 |