Primary Device ID | 04250413401680 |
NIH Device Record Key | ea5c6e7f-5360-4692-a6f0-aad342c1f92c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PLM Sensor Set |
Version Model Number | SOW116 |
Company DUNS | 314112173 |
Company Name | SOMNOmedics 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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04250413401680 [Primary] |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2019-04-12 |
04250413405640 - ABPM pro basic device | 2024-05-16 |
04250413402748 - SOMNOwatch plus ACTI | 2023-12-15 |
04250413402755 - SOMNOwatch plus ACTI | 2023-12-15 |
04250413410781 - SOMNO HD / ECO accessory | 2023-12-08 |
04250413410828 - SOMNOscreen ECO EEG 32 | 2023-12-08 |
04250413410835 - SOMNOtouch RESP accessory | 2023-12-08 |
04250413410842 - SOMNOtouch RESP accessory | 2023-12-08 |
04250413410859 - SOMNOtouch RESP accessory | 2023-12-08 |