Primary Device ID | 07290109145983 |
NIH Device Record Key | 4ee2db3e-3dec-4d0e-b41a-9b5655946707 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lumenis Pulse 30H |
Version Model Number | Lumenis Pulse 30H |
Catalog Number | GA-2003322 |
Company DUNS | 600166524 |
Company Name | LUMENIS 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 | 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 |