Post Op Spectacle Fitover, Clear

GUDID 00818806020388

Post Op Spectacle Fitover, Clear, Small

RXSIGHT, INC.

Tinted spectacle lens, non-prescription Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens Tinted non-prescription spectacle lens
Primary Device ID00818806020388
NIH Device Record Key14727485-3496-4cb0-9db5-7402a88da843
Commercial Distribution Discontinuation2019-08-01
Commercial Distribution StatusNot in Commercial Distribution
Brand NamePost Op Spectacle Fitover, Clear
Version Model Number62012-006
Company DUNS052054413
Company NameRXSIGHT, INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100818806020388 [Primary]

FDA Product Code

HQYSunglasses (Non-Prescription Including Photosensitive)

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-08-15
Device Publish Date2019-04-08

On-Brand Devices [Post Op Spectacle Fitover, Clear]

00818806020388Post Op Spectacle Fitover, Clear, Small
00818806020371Post Op Spectacle Fitover, Clear, Xtra Large
00818806020364Post Op Spectacle Fitover, Clear, Large
00818806020357Post Op Spectacle Fitover, Clear, Medium-Large
00818806020340Post Op Spectacle Fitover, Clear, Medium
00818806020333Post Op Spectacle Fitover, Clear, Medium-Small

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