Suction Cups (12 units)

GUDID 20697660002617

Latex-free Rubber Suction Cups (12 units)

Oculo-Plastik Inc

Corneal shield applicator
Primary Device ID20697660002617
NIH Device Record Key17e23afd-36a4-4cb7-893e-ccab83b7791d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSuction Cups (12 units)
Version Model Number23-012LF
Company DUNS257382580
Company NameOculo-Plastik Inc
Device Count1
DM Exempttrue
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 Latextrue
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone514-381-3292
Emailsales@oculoplastik.com

Device Identifiers

Device Issuing AgencyDevice ID
GS120697660002617 [Primary]

FDA Product Code

KYEInserter/Remover Contact Lens

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[20697660002617]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-11-18
Device Publish Date2019-11-08

Devices Manufactured by Oculo-Plastik Inc

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