Accurus, Alcon

GUDID 10380657410184

Vitrectomy system handpiece

Primary Device ID	10380657410184
NIH Device Record Key	a9950601-6e6a-4ede-8c9b-b00e51744fc4
Commercial Distribution Status	In Commercial Distribution
Brand Name	Accurus, Alcon
Version Model Number	8065741018
Company DUNS	008018525
Company Name	Alcon Laboratories, 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	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	true
RX Perscription	true
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
GS1	00380657410187 [Primary]
GS1	10380657410184 [Package] Contains: 00380657410187 Package: Box [6 Units] In Commercial Distribution

HQC	Unit, phacofragmentation

Steralize Prior To Use	false
Device Is Sterile	true

10380658036505	Anterior Accurus Probe with Infusion Needle
10380657508218	Accurus Standalone 23 GA Vitreous Probe
10380657508140	Combined Procedure Pak with Accurus 23 GA Vitrectomy Probe (0.9 mm Tipless)
10380657410184	Accurus 2500 Stand-Alone Vitreous Probe
10380657407436	Accurus Replacement Drain Bag