Primary Device ID | 00860005082261 |
NIH Device Record Key | e9742657-8538-48ef-b0a3-161b2641b876 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Ceras Health |
Version Model Number | B380 |
Company DUNS | 094681349 |
Company Name | Ceras Health Inc |
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 | false |
Serial Number | true |
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 | 00860005082261 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-01-03 |
Device Publish Date | 2021-12-24 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CERAS HEALTH 86716757 5177211 Live/Registered |
CERAS HEALTH, INC. 2015-08-06 |