HD2

GUDID 08806392040073

Soft corrective contact lens, daily-wear

Primary Device ID	08806392040073
NIH Device Record Key	1ae1ab11-fbdd-4680-93ff-da4c05ae497b
Commercial Distribution Status	In Commercial Distribution
Brand Name	HD2
Version Model Number	HD2
Company DUNS	688455799
Company Name	INTEROJO INC.
Device Count	6
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	true
Serial Number	false
Manufacturing Date	false
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

Phone	+1-760-754-2220
Email	rho@interojo.com

Storage Environment Temperature

Between 1 Degrees Celsius and 30 Degrees Celsius

Device Issuing Agency	Device ID
GS1	08806392040073 [Primary]
GS1	08806392040196 [Unit of Use]

LPL	Lenses, Soft Contact, Daily Wear

Steralize Prior To Use	false
Device Is Sterile	true