FDA UDI In Commercial Distribution 🇺🇸 United States

DRSplus

DI: 08053677040116 · Model: DRSplus · CENTERVUE SPA
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
DRSplus
Primary DI
08053677040116
Version / Model
DRSplus
Company Name
CENTERVUE SPA
Labeler DUNS
338702316
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-09
Public Version
1
Public Version Date
2019-12-17
Public Version Status
New
Public Device Record Key
9d5fc72b-dbaa-4ad0-9e7f-9b1ea8eae888

Device Description

The CenterVue DRSplus is a confocal scanning ophthalmoscope indicated for color imaging of a human retina without the use of a mydriatic agent.

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
Yes
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MYC Ophthalmoscope, Laser, Scanning

GMDN Terms

Code Name
10551 Ophthalmic fundus camera

Identifiers

Type ID
Primary 08053677040116

Premarket Submissions

Submission Number Supplement Number
K192113 000