AcuTip 500

GUDID 00816722022103

Laser skin surface treatment system applicator

Primary Device ID	00816722022103
NIH Device Record Key	e99735e7-3779-466e-b4db-b7484c569c89
Commercial Distribution Status	In Commercial Distribution
Brand Name	AcuTip 500
Version Model Number	AcuTip 500
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	00816722022103 [Primary]

GEX	Powered Laser Surgical Instrument

Steralize Prior To Use	false
Device Is Sterile	false

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00816722021809 - xeo+	2022-12-08 xeo+ Laser System
00816722021816 - xeo+ SA	2022-12-08 xeo+ SA IPL System
00816722022813 - Limelight	2022-12-08 Limelight IPL Handpiece for xeo+/xeo+ SA
00816722022820 - Prowave	2022-12-08 Prowave IPL Handpiece for xeo+/xeo+ SA
00816722022837 - Titan	2022-12-08 Titan IPL Handpiece for xeo+/xeo+ SA
00816722022844 - Pearl Fractional	2022-12-08 Pearl Fractional Laser Handpiece for xeo+/xeo+ SA
00816722022479 - truSculpt 2 RF handpiece	2022-11-22 truSculpt 2 cm^2 handheld handpiece for use with truSculpt iD RF device

Mark Image Registration \| Serial	Company Trademark Application Date
ACUTIP 500 78670925 3199758 Live/Registered	Cutera, Inc. 2005-07-14