Primary Device ID | 07350092810456 |
NIH Device Record Key | 970a548e-251e-4160-bf1f-e5d7d1660109 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sectra Digital Pathology Module |
Version Model Number | 3.3 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07350092810456 [Primary] |
QKQ | Digital Pathology Image Viewing And Management Software |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-06-29 |
Device Publish Date | 2023-06-21 |
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 |