DUOVISC

GUDID 00380651999077

DuoVisc Viscoelastic System

Alcon Laboratories, Inc.

Aqueous/vitreous humour replacement medium kit
Primary Device ID00380651999077
NIH Device Record Keyea207a6a-7dcc-45c4-a69f-6086a01eb857
Commercial Distribution StatusIn Commercial Distribution
Brand NameDUOVISC
Version Model Number8065199907
Company DUNS008018525
Company NameAlcon Laboratories, Inc.
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)862-5266
Emailweb.masterus@alcon.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100380651999077 [Primary]

FDA Product Code

LZPAID, SURGICAL, VISCOELASTIC

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 Date2017-11-14

On-Brand Devices [DUOVISC]

00380651999077DuoVisc Viscoelastic System
00380651831506DUOVISC (0.55PRO/0.50VIS)
00380651831353DUOVISC (0.40PRO/0.35VIS)

Trademark Results [DUOVISC]

Mark Image

Registration | Serial
Company
Trademark
Application Date
DUOVISC
DUOVISC
74183443 1895532 Live/Registered
ALCON RESEARCH, LTD.
1991-07-09

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.