Primary Device ID | 00786511834203 |
NIH Device Record Key | 38b624dd-b4c0-41e9-9703-00516adc0d30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Otoscope |
Version Model Number | 3420-ROY |
Company DUNS | 078803608 |
Company Name | RASHMAN CORPORATION |
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 | false |
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 | 00786511834203 [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 | 2022-12-14 |
Device Publish Date | 2022-12-06 |
00786511834203 | Standard Pocket Otoscope |
00786511786809 | Mini OtoLite Otoscope |
00786511392444 | Xenon Pocket Otoscope |
00786511034207 | Standard Pocket Otoscope |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
OTOSCOPE 77875618 3905524 Live/Registered |
Smith, Richard J.H. 2009-11-18 |