ProWave LX

GUDID 00816722022134

Laser skin surface treatment system applicator

Primary Device ID	00816722022134
NIH Device Record Key	1e4f92fd-65dd-4713-a4e1-47a5cf1eefe2
Commercial Distribution Status	In Commercial Distribution
Brand Name	ProWave LX
Version Model Number	ProWave LX
Company DUNS	041071643
Company Name	CUTERA, INC.
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

Device Issuing Agency	Device ID
GS1	00816722022134 [Primary]

GEX	Powered Laser Surgical Instrument

Steralize Prior To Use	false
Device Is Sterile	false

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