FDA UDI Not in Commercial Distribution 🇺🇸 United States

HD2

DI: 08806392040073 · Model: HD2 · INTEROJO INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
6

Basic Information

Brand Name
HD2
Primary DI
08806392040073
Version / Model
HD2
Company Name
INTEROJO INC.
Labeler DUNS
688455799
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
6
Record Status
Published
Publish Date
2020-02-03
Public Version
2
Public Version Date
2020-06-09
Public Version Status
Update
Public Device Record Key
1ae1ab11-fbdd-4680-93ff-da4c05ae497b
Distribution End Date
2020-06-07

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LPL Lenses, Soft Contact, Daily Wear

GMDN Terms

Code Name
47842 Soft corrective contact lens, daily-wear

Identifiers

Type ID
Primary 08806392040073
Unit of Use 08806392040196

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K080794 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
1 – 30 Degrees Celsius