Primary Device ID | 04033817901587 |
NIH Device Record Key | 6d7b8f77-a11b-4b78-9637-fb3989ee15e4 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Connect |
Version Model Number | Recorder |
Company DUNS | 343225272 |
Company Name | LivaNova Deutschland GmbH |
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 | true |
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 | 04033817901587 [Primary] |
DXJ | DISPLAY, CATHODE-RAY TUBE, MEDICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2024-05-07 |
Device Publish Date | 2016-05-30 |
04033817901587 | Recorder |
04033817901570 | Manager |