Primary Device ID | 00073796416027 |
NIH Device Record Key | dd472439-ed8b-4e0a-9bff-085747769ecd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Omron Sprague Rappaport Stethoscope |
Version Model Number | 416-22-DB |
Catalog Number | 416-22-DB |
Company DUNS | 054318779 |
Company Name | Omron Healthcare, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com | |
Phone | 800-634-4350 |
ohiquality@omron.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00073796416027 [Primary] |
LDE | Stethoscope, Manual |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-07-21 |
Device Publish Date | 2020-07-13 |
00073796416027 | Stethoscope, high luster, chrome plated binaural with long life rugged 22 inch double tubing, Da |
00073796416003 | Stethoscope Black, high luster chrome plated binaural with long life rugged 22 inch double tube. |