| 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 |