Xpeeda™ ENDO D/S/L AC-10000730

GUDID 07290109145808

General/multiple surgical laser system beam guide, single-use

Primary Device ID	07290109145808
NIH Device Record Key	be67a9bc-86a7-4647-b347-c5b8d444c507
Commercial Distribution Status	In Commercial Distribution
Brand Name	Xpeeda™ ENDO D/S/L
Version Model Number	Xpeeda™ ENDO D/S/L
Catalog Number	AC-10000730
Company DUNS	600166524
Company Name	LUMENIS 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	true
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	07290109145808 [Primary]

GEX	Powered Laser Surgical Instrument

Steralize Prior To Use	false
Device Is Sterile	true