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EUDAMED registration 16975631346098No

Suction head

JIANGSU COMEON MEDICAL APPARATUS CO., LTDClass AEU EUDAMED
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class A
CND nomenclatures code
W0599
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
16975631346098
Basic UDI
697563134KM006G2
Version date
January 11, 2023
Manufacturer last update
December 23, 2021
Active status
No
Manufacturer
Manufacturer name
JIANGSU COMEON MEDICAL APPARATUS CO., LTD
Country
China
Country type
NON_EU
Address
No. 18, Guanzhuang East Road, Jiangyan District, Taizhou City, Jiangsu Province
Email
68263536@qq.com
Authorized representative
Name
Sungo Cert GmbH
SRN
DE-AR-000010869
Country
Germany
Address
47 Harffstr. Düsseldorf
Email
de.rep@sungoglobal.com
Regulatory information
Competent authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed on the market
Austria
Market available
Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia: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)

IVD GENERAL USE CONSUMABLE DEVICES - OTHER

About this record

Access comprehensive regulatory information for Suction head in the European Union medical device market through Pure Global AI's free database. This Class A device is registered with EU EUDAMED under Primary DI 16975631346098 and manufactured by JIANGSU COMEON MEDICAL APPARATUS CO., LTD in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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.