Primary Device ID | 07350092810500 |
NIH Device Record Key | 54f755bc-8da0-45e0-bfe6-e66e7d37a60e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sectra Digital Pathology Module |
Version Model Number | 4.0 |
Company DUNS | 354117848 |
Company Name | Sectra AB |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
07350092810197 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810289 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810333 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810388 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810425 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810456 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810487 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810500 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |
07350092810524 | For In Vitro Diagnostic Use
Sectra Digital Pathology Module device is a software intended for vi |