FDA UDI Not in Commercial Distribution 🇺🇸 United States

Post Op Spectacle Fitover, Tinted

DI: 00818806020401 · Model: 62013-002 · RXSIGHT, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Post Op Spectacle Fitover, Tinted
Primary DI
00818806020401
Version / Model
62013-002
Company Name
RXSIGHT, INC.
Labeler DUNS
052054413
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-04-08
Public Version
3
Public Version Date
2023-05-02
Public Version Status
Update
Public Device Record Key
67b85383-e95b-4284-a33a-0fd717ff907e
Distribution End Date
2023-05-01

Device Description

Post Op Spectacle Fitover, Tinted, Medium

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

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
HQY Sunglasses (Non-Prescription Including Photosensitive)

GMDN Terms

Code Name
46297 Tinted non-prescription spectacle lens

Identifiers

Type ID
Primary 00818806020401