Primary Device ID | B141MEDISSUITEXA20200 |
NIH Device Record Key | 2ece4459-b625-4ea4-a02f-f999e5d1ae5a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Medis Suite XA |
Version Model Number | 2020 |
Company DUNS | 549961191 |
Company Name | Medis Medical Imaging Systems B.V. |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B141MEDISSUITEXA20190 [Previous] |
HIBCC | B141MEDISSUITEXA20200 [Primary] |
LLZ | System, Image Processing, Radiological |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-09-21 |
Device Publish Date | 2020-09-11 |
B141MEDISSUITEXA20200 | Medis Suite XA is indicated for use in clinical settings where validated and reproducible quanti |
B141MEDISSUITEXA20210 | Medis Suite XA is indicated for use in clinical settings where validated and reproducible quanti |
B141MEDISSUITEXA20220 | Medis Suite XA 2022 is indicated for use in clinical settings where validated and reproducible q |
B141MEDISSUITEXA20230 | Medis Suite XA 2023 is indicated for use in clinical settings where validated and reproducible q |