Primary Device ID | 00817495023946 |
NIH Device Record Key | beba8331-ee66-40ba-9da7-9827028f869d |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Modified LSDS Fiber Assembly, 12-26 mm |
Version Model Number | SBA100775 |
Catalog Number | SBA100775 |
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 | 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 |
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