Primary Device ID | 07290102932733 |
NIH Device Record Key | 12167289-3ae8-4b45-9ec3-e56c317b95b7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ensemble |
Version Model Number | 555-000-280 |
Catalog Number | 555-000-280 |
Company DUNS | 600019749 |
Company Name | MENNEN MEDICAL LTD. |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | +2152591020 |
info@mmi.co.il |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07290102932733 [Primary] |
DSI | Detector And Alarm, Arrhythmia |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2016-09-24 |
07290102932320 - VitaLogik4000 | 2020-02-06 Patient monitor |
07290102932474 - Menntor | 2020-02-06 Patient monitor |
07290102932481 - Menntor | 2020-02-06 Patient monitor |
07290102932498 - VitaLogik4000 | 2020-02-06 Patient monitor |
07290102932504 - VitaLogik4000 | 2020-02-06 Patient monitor |
07290102932511 - VitaLogik4500 | 2020-02-06 Patient monitor |
07290102932528 - VitaLogik4500 | 2020-02-06 Patient monitor |
07290102932535 - VitaLogik4500 | 2020-02-06 Patient monitor |