23ga Bending Laser Probe - Iridex Compatible VS0140.23I

GUDID B384VS014023I5

Ophthalmic laser system beam guide

Primary Device ID	B384VS014023I5
NIH Device Record Key	44f19584-23a1-4bea-9295-fbbb3aa361ea
Commercial Distribution Status	In Commercial Distribution
Brand Name	23ga Bending Laser Probe - Iridex Compatible
Version Model Number	VS0140.23I
Catalog Number	VS0140.23I
Company DUNS	080375891
Company Name	VORTEX SURGICAL, LLC
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	true
RX Perscription	false
OTC Over-The-Counter	false

Device Issuing Agency	Device ID
HIBCC	B384VS014023I1 [Primary]
HIBCC	B384VS014023I5 [Package] Contains: B384VS014023I1 Package: Box [10 Units] In Commercial Distribution

HQB	Photocoagulator And Accessories

Steralize Prior To Use	false
Device Is Sterile	true

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