Pure Global

LogiTube Gastric Calibration Tube - EUDAMED Registration 05051986013565

Access comprehensive regulatory information for LogiTube Gastric Calibration Tube 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 05051986013565 and manufactured by Surgical Innovations Ltd. in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (LogiTube Gastric Calibration Tube ), 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.

Free Database
Powered by Pure Global AI
EUDAMED Official Data
Class I
05051986013565
No
LogiTube Gastric Calibration Tube
Trade Name: LogiTube Gastric Calibration Tube
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

GASTRIC CALIBRATION TUBES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
G020502
Trade Name
LogiTube Gastric Calibration Tube
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
05051986013565
Basic UDI
5051986SISUG4H
Version Date
February 27, 2025
Manufacturer Last Update
August 25, 2021
Active Status
No
Manufacturer
Manufacturer Name
Surgical Innovations Ltd.
Country
United Kingdom (ex Northern Ireland)
Country Type
NON_EU
Address
6 Clayton Wood House, Clayton Wood Bank Leeds
Email
si@surginno.co.uk
Authorized Representative
SRN
IE-AR-000004113
Country
Ireland
Address
The Black Church Dublin
Email
edwin@cslifesciences.com
Telephone
+447917134922
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
Ireland
Market Available
Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Ireland:None~None, Italy:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Tรผrkiye:None~None, United Kingdom (Northern Ireland only):None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No