DURAPLUG

GUDID 00844505007269

DURAPLUG SYNTHETIC ABSORBABLE EXTENDED WEAR PLUGS 0.4MM DIAMETER X 2.0MM LENGTH

EAGLE VISION, INC.

Lacrimal punctum plug
Primary Device ID00844505007269
NIH Device Record Keydad6af6f-3e6e-4e93-91a3-cacf2862ebf1
Commercial Distribution Discontinuation2017-03-31
Commercial Distribution StatusNot in Commercial Distribution
Brand NameDURAPLUG
Version Model Number0078
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
GS100844505007269 [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 [DURAPLUG]

00844505007269DURAPLUG SYNTHETIC ABSORBABLE EXTENDED WEAR PLUGS 0.4MM DIAMETER X 2.0MM LENGTH
00844505007252DURAPLUG SYNTHETIC ABSORBABLE EXTENDED WEAR PLUGS 0.3MM DIAMETER X 2.0MM LENGTH
00844505007245DURAPLUG SYNTHETIC ABSORBABLE EXTENDED WEAR PLUGS 0.2MM DIAMETER X 2.0MM LENGTH

Trademark Results [DURAPLUG]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DURAPLUG
DURAPLUG
78570293 3276631 Live/Registered
KATENA PRODUCTS, INC.
2005-02-18
DURAPLUG
DURAPLUG
75960485 not registered Dead/Abandoned
ALCON, INC.
2000-03-16

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