Beaver-Visitec MMK967

GUDID 05055186240066

Malosa Core SMILE Pack 2-Beaver-Visitec International Ltd (30/SP)

Beaver-Visitec International, Inc.

Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use Ophthalmic surgical procedure kit, non-medicated, single-use
Primary Device ID05055186240066
NIH Device Record Key16ac149a-1961-4813-b3bf-37f517394fb1
Commercial Distribution StatusIn Commercial Distribution
Brand NameBeaver-Visitec
Version Model NumberMMK967
Catalog NumberMMK967
Company DUNS001406024
Company NameBeaver-Visitec International, Inc.
Device Count30
DM Exemptfalse
Pre-market Exempttrue
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 Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com
Phone18669068080
Emailcustomersupport@beaver-visitec.com

Device Identifiers

Device Issuing AgencyDevice ID
GS105055186240066 [Unit of Use]
GS130551862400664 [Primary]
GS135055186240661 [Primary]

FDA Product Code

PZGSurgical Eye Tray

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-23
Device Publish Date2021-11-15

On-Brand Devices [Beaver-Visitec]

05055186237981Malosa Core Phaco Pack 1 (30/SP)
05055186236953Malosa Core SMILE Pack 1 (20/SP)
05055186236069Malosa Core Suface Treatment Pack (20/SP)
05055186236052Malosa Core LASIK Pack 2 (20/SP)
05055186235833Malosa Core Phaco Pack 2 (30/SP)
05055186240066Malosa Core SMILE Pack 2-Beaver-Visitec International Ltd (30/SP)

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