FDA UDI In Commercial Distribution 🇺🇸 United States

OPTICAL BIOMETER

DI: 04573344510017 · Model: ARGOS · SANTEC CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OPTICAL BIOMETER
Primary DI
04573344510017
Version / Model
ARGOS
Company Name
SANTEC CORPORATION
Labeler DUNS
704295641
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-05-01
Public Version
4
Public Version Date
2019-08-09
Public Version Status
Update
Public Device Record Key
2ccd1453-e889-45b1-9c6e-cdf508056060

Device Description

ARGOS is a non-invasive, non-contact biometer based on swept-source optical coherence tomography (SS-OCT). The device is intended to acquire ocular measurements as well as perform calculations to determine the appropriate intraocular lens (IOL) power and type for implantation during intraocular lens placement. ARGOS measures the following 9 parameters: Axial Length, Corneal Thickness, Anterior Chamber Depth, Lens Thickness, K-values (Radii of flattest and steepest meridians), Astigmatism, Whiteto- white (corneal diameter) and Pupil Size. It is intended for use by ophthalmologists, physicians, and other eye-care professionals and may only be used under the supervision of a physician.

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
MR Unsafe
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
MXK Device,Analysis,Anterior Segment

GMDN Terms

Code Name
12811 Bench-top keratometer

Identifiers

Type ID
Primary 04573344510017

Premarket Submissions

Submission Number Supplement Number
K150754 000