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EUDAMED registration 05060396170171Yes

OTOPORT OTOCHECK LE TE

OTODYNAMICS LTDClass IIaEU EUDAMEDTrade name: Otodynamics
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class IIa
CND nomenclatures code
Z12149001
Trade name
Otodynamics
Implantable
No
Reusable
No
Measuring function
Yes
Registration information
Primary DI
05060396170171
Basic UDI
B-05060396170171
Version date
March 23, 2022
Manufacturer last update
January 13, 2022
Active status
Yes
Manufacturer
Manufacturer name
OTODYNAMICS LTD
Country
United Kingdom (ex Northern Ireland)
Country type
NON_EU
Address
30-38 Beaconsfield Road Hatfield
Email
support@otodynamics.com
Authorized representative
Name
Medical Device Safety Service GmbH (MDSS)
SRN
DE-AR-000005430
Country
Germany
Address
41 Schiffgraben Hannover
Email
info@mdssar.com
Regulatory information
Competent authority
DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover
Applicable legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed on the market
Germany
Market available
Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czech Republic:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Turkey:None~None, United Kingdom (Northern Ireland only):None~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

OTOACOUSTIC EMISSIONS EQUIPMENT

About this record

Access comprehensive regulatory information for OTOPORT OTOCHECK LE TE 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 05060396170171 and manufactured by OTODYNAMICS LTD in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Otodynamics), manufacturer information, authorized representative details, competent authority (DE/CA09 - Staatliches Gewerbeaufsichtsamt Hannover), 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.