Profound, Dermal Single- Use Cartridge, Packaged

GUDID 00817495024387

Multi-modality skin surface treatment system

Primary Device ID	00817495024387
NIH Device Record Key	7d3c738a-b5aa-4f58-a770-54c600d77ac0
Commercial Distribution Status	In Commercial Distribution
Brand Name	Profound, Dermal Single- Use Cartridge, Packaged
Version Model Number	AS77795
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	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	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00817495024387 [Primary]

GEI	Electrosurgical, Cutting & Coagulation & Accessories

Steralize Prior To Use	false
Device Is Sterile	true