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EUDAMED registration 00850011743836No

CANNULA

Med-Logics, Inc.Class IIaEU EUDAMED
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
Z1212020785
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
00850011743836
Basic UDI
B-00850011743836
Version date
January 18, 2024
Manufacturer last update
May 19, 2021
Active status
No
Manufacturer
Manufacturer name
Med-Logics, Inc.
Country
United States
Country type
NON_EU
Address
1627 Enterprise Street 75751 Athens
Email
Justin.Ross@mlogics.com
Authorized representative
Name
E C REP LIMITED
SRN
IE-AR-000003995
Country
Ireland
Address
5 Fitzwilliam Square East Dublin D2
Email
info@ecrep.ie
Telephone
+353 89 225 1951
Regulatory information
Competent authority
Health Products Regulatory Authority, Medical Devices Department
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
Ireland
Market available
Austria:2008-01-01~2044-01-01, Belgium:2008-01-01~2044-01-01, Bulgaria:2008-01-01~2044-01-01, Croatia:2008-01-01~2044-01-01, Cyprus:2008-01-01~2044-01-01, Czechia:2008-01-01~2044-01-01, Denmark:2008-01-01~2044-01-01, Estonia:2008-01-01~2044-01-01, Finland:2008-01-01~2044-01-01, France:2008-01-01~2044-01-01, Germany:2008-01-01~2044-01-01, Greece:2008-01-01~2044-01-01, Hungary:2008-01-01~2044-01-01, Iceland:2008-01-01~2044-01-01, Ireland:2008-01-01~2044-01-01, Italy:2008-01-01~2044-01-01, Latvia:2008-01-01~2044-01-01, Liechtenstein:2008-01-01~2044-01-01, Lithuania:2008-01-01~2044-01-01, Luxembourg:2008-01-01~2044-01-01, Malta:2008-01-01~2044-01-01, Netherlands:2008-01-01~2044-01-01, Norway:2008-01-01~2044-01-01, Poland:2008-01-01~2044-01-01, Portugal:2008-01-01~2044-01-01, Romania:2008-01-01~2044-01-01, Slovakia:2008-01-01~2044-01-01, Slovenia:2008-01-01~2044-01-01, Spain:2008-01-01~2044-01-01, Sweden:2008-01-01~2044-01-01, Turkey:2008-01-01~2044-01-01, United Kingdom (Northern Ireland only):2008-01-01~2044-01-01
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

PHACO-VITRECTOMY INSTRUMENTS - CONSUMABLES

About this record

Access comprehensive regulatory information for CANNULA in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 00850011743836 and manufactured by Med-Logics, Inc. in United States.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.