Lacrimal Plug

GUDID 00812444028782

Canalicular Plug

RIVERPOINT MEDICAL, LLC

Lacrimal punctum plug
Primary Device ID00812444028782
NIH Device Record Key467f9bdd-4704-46f6-a0d9-ba647e940f13
Commercial Distribution StatusIn Commercial Distribution
Brand NameLacrimal Plug
Version Model NumberESK-1005
Company DUNS964053560
Company NameRIVERPOINT MEDICAL, LLC
Device Count1
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 Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100812444028782 [Primary]
GS110812444028789 [Package]
Package: [10 Units]
In Commercial Distribution

FDA Product Code

LZUPlug, Punctum

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-04-12
Device Publish Date2018-10-01

On-Brand Devices [Lacrimal Plug]

00812444028782Canalicular Plug
00812444028775Canalicular Plug
00812444028768Canalicular Plug
00812444028744Canalicular Plug
10840277405125CANALICULAR PLUG
10840277405118CANALICULAR PLUG
10840277405101CANALICULAR PLUG
10840277405095CANALICULAR PLUG

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