Primary Device ID | 00817495022871 |
NIH Device Record Key | 89da4c01-67d0-494a-a407-6f3bff9cf107 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Kit, PicoWay 730nm Handpiece |
Version Model Number | 7123-00-0590 |
Company DUNS | 053468385 |
Company Name | CANDELA CORPORATION |
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 | true |
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 |