20ga Widefield Light Pipe

GUDID 10817489025649

20ga Widefield Light Pipe

KATALYST SURGICAL LLC

Ophthalmic laser system beam guide
Primary Device ID10817489025649
NIH Device Record Key9a74cf04-b282-4359-8997-3c84449f84ec
Commercial Distribution Discontinuation2025-07-01
Commercial Distribution StatusNot in Commercial Distribution
Brand Name20ga Widefield Light Pipe
Version Model NumberV2010-20R
Company DUNS007883297
Company NameKATALYST SURGICAL LLC
Device Count10
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100817489025642 [Unit of Use]
GS110817489025649 [Primary]

FDA Product Code

MPAEndoilluminator

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2025-07-03
Device Publish Date2017-10-13

On-Brand Devices [20ga Widefield Light Pipe]

1081748902565620ga Widefield Light Pipe
1081748902564920ga Widefield Light Pipe

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