SUPEREAGLE

GUDID 00844505010542

SUPEREAGLE PUNCTUM PLUG LARGE SILICONE TWIN PACK

EAGLE VISION, INC.

Lacrimal punctum plug
Primary Device ID00844505010542
NIH Device Record Key5b77ec24-876b-44d9-85db-af49258d3509
Commercial Distribution Discontinuation2017-03-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameSUPEREAGLE
Version Model Number31322
Company DUNS174318360
Company NameEAGLE VISION, INC.
Device Count1
DM Exempttrue
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 Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone1-800-222-7584
Emailinfo@eaglevis.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100844505010542 [Primary]

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 Date2018-03-29
Device Publish Date2016-09-26

On-Brand Devices [SUPEREAGLE]

00844505010559SUPEREAGLE PUNCTUM PLUG MEDIUM SILICONE TWIN PACK
00844505010542SUPEREAGLE PUNCTUM PLUG LARGE SILICONE TWIN PACK
00844505010535SUPEREAGLE PUNCTUM PLUG SMALL SILICONE TWIN PACK

Trademark Results [SUPEREAGLE]

Mark Image

Registration | Serial
Company
Trademark
Application Date
SUPEREAGLE
SUPEREAGLE
77361471 3476424 Live/Registered
KATENA PRODUCTS, INC.
2007-12-29

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