Primary Device ID | 37290109951196 |
NIH Device Record Key | f5f6566f-21be-4b54-a5ff-a306df7b586e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Standard 64 Sublative iD, (200 Pulse), 10-Pk |
Version Model Number | KT72931 |
Catalog Number | KT72931 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
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