FDA UDI In Commercial Distribution 🇺🇸 United States

TrueTear

DI: 00850102007137 · Model: F-0030 · OCULEVE, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
30

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
TrueTear
Primary DI
00850102007137
Version / Model
F-0030
Catalog Number
F-0030
Company Name
OCULEVE, INC.
Labeler DUNS
078797682
Distribution Status
In Commercial Distribution
Device Count in Pkg
30
Record Status
Published
Publish Date
2017-06-29
Public Version
3
Public Version Date
2021-05-24
Public Version Status
Update
Public Device Record Key
a9e494ee-d83b-4fdd-bbed-8f5689d81714

Device Description

TrueTear Disposable Tip

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
PQJ Intranasal electrostimulation device

GMDN Terms

Code Name
62549 Intranasal lacrimal electrical neurostimulator electrode

Identifiers

Type ID
Primary 00850102007137
Unit of Use 10850102007134

Customer Contacts

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 40 Degrees Celsius