Primary Device ID | 10856602005021 |
NIH Device Record Key | edc4c49e-a399-4ee8-b51d-bbfed499b4f7 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | SPC-0572.B02 |
Company DUNS | 149825791 |
Company Name | PROTEUS DIGITAL HEALTH, INC. |
Device Count | 2 |
DM Exempt | true |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
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 | 00856602005024 [Unit of Use] |
GS1 | 10856602005021 [Primary] |
DXH | TRANSMITTERS AND RECEIVERS, ELECTROCARDIOGRAPH, TELEPHONE |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2022-11-28 |
Device Publish Date | 2016-07-07 |
10856602005021 - NA | 2022-11-28 |
10856602005021 - NA | 2022-11-28 |
10856602005045 - NA | 2022-11-28 |
10856602005052 - NA | 2022-11-28 |
10856602005069 - NA | 2022-11-28 |
10856602005076 - NA | 2022-11-28 |
10856602005083 - NA | 2022-11-28 |
10856602005090 - NA | 2022-11-28 |
10856602005106 - NA | 2022-11-28 |