Beaver-Visitec MMK110/3

GUDID 05055186236069

Malosa Core Suface Treatment Pack (20/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
Primary Device ID05055186236069
NIH Device Record Keya535b9de-638b-448b-b422-b4895d9ff65d
Commercial Distribution StatusIn Commercial Distribution
Brand NameBeaver-Visitec
Version Model NumberMMK110/3
Catalog NumberMMK110/3
Company DUNS001406024
Company NameBeaver-Visitec International, Inc.
Device Count20
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

Device Identifiers

Device Issuing AgencyDevice ID
GS105055186236069 [Unit of Use]
GS135055186236060 [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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