Primary Device ID | 07290109951614 |
NIH Device Record Key | 126794aa-106c-4928-a7c0-6c8ba08f5b84 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AC applicator |
Version Model Number | FG70591R |
Catalog Number | FG70591R |
Company DUNS | 532685716 |
Company Name | SYNERON MEDICAL LTD |
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 |