Microsmooth, Alcon

GUDID 10380657505187

1.1mm Microsmooth ULTRA Infusion Sleeve Kit

Alcon Laboratories, Inc.

Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use
Primary Device ID10380657505187
NIH Device Record Key440b04bc-3928-4b11-9164-68f25387173a
Commercial Distribution StatusIn Commercial Distribution
Brand NameMicrosmooth, Alcon
Version Model Number8065750518
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
Phone+1(800)862-5266
Emailweb.masterus@alcon.com

Device Dimensions

Outer Diameter1.1 Millimeter
Outer Diameter1.1 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
GS100380657505180 [Primary]
GS110380657505187 [Package]
Contains: 00380657505180
Package: Box [6 Units]
In Commercial Distribution

FDA Product Code

HQCUnit, phacofragmentation

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2019-11-08
Device Publish Date2016-09-24

On-Brand Devices [Microsmooth, Alcon]

103806575051941.1mm Micromooth MICRO
103806575051871.1mm Microsmooth ULTRA Infusion Sleeve Kit
103806574087231.1mm MicroSmooth HIGH INFUSION SLEEVE PARTS KIT
103806574084260.9mm Microsmooth HIGH INFUSION SLEEVE PARTS KIT

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