Primary Device ID | 10073796341722 |
NIH Device Record Key | 8b9f3ccc-9cef-4afa-9ff4-33cdb999e9d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omron Wide Range D-ring Cuff |
Version Model Number | HEM-RML31-B |
Catalog Number | HEM-RML31-B |
Company DUNS | 054318779 |
Company Name | Omron Healthcare, 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 | 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 | true |
Phone | 1-800-634-4350 |
ohiquality@omron.com |
Handling Environment Temperature | Between 50 Degrees Fahrenheit and 104 Degrees Fahrenheit |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00073796341725 [Primary] |
GS1 | 10073796341722 [Package] Contains: 00073796341725 Package: Case [20 Units] In Commercial Distribution |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-07-22 |
Device Publish Date | 2019-04-03 |
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