FDA UDI In Commercial Distribution 🇺🇸 United States

RxSight Insertion Device

DI: 10818806021016 · Model: 63002 · RXSIGHT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
10

Basic Information

Brand Name
RxSight Insertion Device
Primary DI
10818806021016
Version / Model
63002
Company Name
RXSIGHT, INC.
Labeler DUNS
052054413
Distribution Status
In Commercial Distribution
Device Count in Pkg
10
Record Status
Published
Publish Date
2024-11-12
Public Version
1
Public Version Date
2024-11-20
Public Version Status
New
Public Device Record Key
cbf09047-e9c2-47f0-8fe7-7b372e913776

Device Description

RxSight Insertion Device (Single-Use)

Device Characteristics

Single Use
Yes
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
No
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
MSS Folders And Injectors, Intraocular Lens (Iol)

GMDN Terms

Code Name
47725 Manual intraocular lens injector, single-use

Identifiers

Type ID
Unit of Use 00818806021019
Primary 10818806021016

Premarket Submissions

Submission Number Supplement Number
K231838 000

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
5 – 30 Degrees Celsius