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Sample container - EUDAMED Registration 05055382309703

Access comprehensive regulatory information for Sample container 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 05055382309703 and manufactured by Reliance Medical Ltd in United Kingdom (ex Northern Ireland).

This page provides complete registration details including trade name (Alvita Specimen Container 60ML), 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.

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EUDAMED Official Data
Class A
05055382309703
No
Sample container
Trade Name: Alvita Specimen Container 60ML
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Device Description (EMDN)

URINE COLLECTION, CONTAINERS

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W05010203
Trade Name
Alvita Specimen Container 60ML
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
05055382309703
Basic UDI
506013188TF6444
Version Date
January 23, 2025
Manufacturer Last Update
September 12, 2023
Active Status
No
Manufacturer
Manufacturer Name
Reliance Medical Ltd
Country
United Kingdom (ex Northern Ireland)
Country Type
NON_EU
Address
West Avenue Stoke on Trent
Email
regulatory@reliancemedical.co.uk
Authorized Representative
SRN
IE-AR-000003675
Country
Ireland
Address
Unit 17 Kylemore Road Dublin
Email
regulatory@reliancemedical.co.uk
Telephone
+44 8456 448808
Regulatory Information
Competent Authority
Health Products Regulatory Authority, Medical Devices Department
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Ireland
Device Characteristics
Human Tissues
No
Animal Tissues
No