| Primary Device ID | 06944413806733 |
| NIH Device Record Key | 01888724-562f-4e08-b529-8dfae36c1af0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ultrasonic Pocket Doppler |
| Version Model Number | PD-100A |
| Company DUNS | 529173163 |
| Company Name | Edan Instruments, 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 | true |
| Expiration Date | false |
| 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 | 06944413806733 [Primary] |
| KNG | Monitor, Ultrasonic, Fetal |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2016-09-01 |
| 06944413808751 | SD1 |
| 06944413806795 | PD-1000 Plus |
| 06944413806788 | PD-1000 |
| 06944413806771 | PD-100 Pro |
| 06944413806764 | PD-100 Plus |
| 06944413806757 | PD-1000 Pro |
| 06944413806740 | PD-100B |
| 06944413806733 | PD-100A |
| 06944413802032 | SD3 Vascular |
| 06944413801813 | SD3 PRO |
| 06944413801806 | SD3 PLUS |
| 06944413801790 | SD3 LITE |
| 06944413801783 | SD3 |
| 06944413800564 | SONOTRAX Vascular |
| 06944413800175 | SONOTRAX Ⅱ Pro |
| 06944413800168 | SONOTRAX Ⅱ |
| 06944413800151 | SONOTRAX Pro |
| 06944413800144 | SONOTRAX Basic A |
| 06944413800137 | SONOTRAX Basic |
| 06944413800120 | SONOTRAX Lite |