FDA UDI In Commercial Distribution 🇺🇸 United States

MOPTIM

DI: 06972039971641 · Model: DEA · Shenzhen CERTAINN Technology Co., Ltd.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
MOPTIM
Primary DI
06972039971641
Version / Model
DEA
Company Name
Shenzhen CERTAINN Technology Co., Ltd.
Labeler DUNS
526992561
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-12-08
Public Version
1
Public Version Date
2022-12-16
Public Version Status
New
Public Device Record Key
a3bc689f-2a3e-4878-b40b-8ebdede82e67

Device Description

The DEA is intended to do the exams related to the analysis and possible diagnosis of Dry Eye Disease(DED) through the connection of the device to you pc, and particularly. • Interferometry: records a video to the patient’s eye to analyze quantitatively and qualitatively lipid layer of the tear film, to compare it with the related grading scale and save the value; • Tear Meniscus Hight: The tear secretion of the lacrimal layer was assessed by measuring the height of the tear meniscus; • NIBUT: recording a video, it allows to evaluate the stability of the tear film between the break up time in a non-invasive way and to save the value; • Fluorescein BUT: records a video for the evaluation of the tear film’s stability, but it is done with instillation of the fluorescein in the patient’s eye (invasive) and without cone; • Meibography: takes a picture of meibomian glands using infrared light. The device can analyze automatically the loss area of the glands to compare it with the related grading scale; • Additional exams: checks for Bulbar Redness, Blepharitis, Demodex, pupillometry. All the exams that can be performed with the DEA are of fundamental importance for the ophthalmologist and the optometrist (within their respective professional skins) to study the tear film and for coaching the exams done with the classic instruments (Slit Lamp, Topography, Tonometry, etc.).

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
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
Yes
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HLR Keratoscope, Battery-Powered

GMDN Terms

Code Name
62593 Meibomian gland camera/ophthalmic interferometer

Identifiers

Type ID
Primary 06972039971641

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
-20 – 55 Degrees Celsius
Type
Storage Environment Humidity
Temperature Range
0 – 93 Percent (%) Relative Humidity
Type
Storage Environment Atmospheric Pressure
Temperature Range
86 – 106 KiloPascal
Type
Handling Environment Temperature
Temperature Range
5 – 40 Degrees Celsius
Type
Handling Environment Humidity
Temperature Range
0 – 80 Percent (%) Relative Humidity
Type
Handling Environment Atmospheric Pressure
Temperature Range
86 – 106 KiloPascal