Pure Global AI
EUDAMED registration 05060671730670No

Endoscopy Cart

Endocarts International LimitedClass IEU EUDAMEDTrade name: Endotrans 6 tray cart (no tray) 
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
V9099
Trade name
Endotrans 6 tray cart (no tray) 
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
05060671730670
Basic UDI
506067173ENDC000001RM
Version date
January 13, 2025
Manufacturer last update
December 16, 2024
Active status
No
Manufacturer
Manufacturer name
Endocarts International Limited
Country
United Kingdom (ex Northern Ireland)
Country type
NON_EU
Address
55 Vanguard Way Essex
Email
QARA@endocartsinternational.com
Authorized representative
Name
Acorn Regulatory Consultancy Services Ltd
SRN
IE-AR-000000592
Country
Ireland
Address
Knockmorris Co. Tipperary
Email
prrc@acornregulatory.com
Telephone
+ 353 52 6176706
Regulatory information
Competent authority
Health Products Regulatory Authority, Medical Devices Department
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
France
Market available
Belgium:2018-12-01~None, Denmark:2018-12-01~None, France:2018-12-01~None, Greece:2018-12-01~None, Ireland:2018-12-01~None, Italy:2018-12-01~None, Norway:2018-12-01~None, Poland:2018-12-01~None, Portugal:2018-12-01~None, Spain:2018-12-01~None
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER

About this record

Access comprehensive regulatory information for Endoscopy Cart in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 05060671730670 and manufactured by Endocarts International Limited in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Endotrans 6 tray cart (no tray) ), 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.