Pure Global

Immunochemistry Systems CAL 2 Calibrator 2 - EUDAMED Registration 15099590232634

Access comprehensive regulatory information for Immunochemistry Systems CAL 2 Calibrator 2 in the European Union medical device market through Pure Global AI's free database. This Class B device is registered with EU EUDAMED under Primary DI 15099590232634 and manufactured by Beckman Coulter Inc. in United States.

This page provides complete registration details including trade name (Immunochemistry Systems CAL 2 Calibrator 2), 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 B
15099590232634
No
Immunochemistry Systems CAL 2 Calibrator 2
Trade Name: Immunochemistry Systems CAL 2 Calibrator 2
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

SPECIFIC PROTEIN STANDARDS AND CALIBRATORS

Device Classification
Risk Class
Class B
CND Nomenclatures Code
W0102152203
Trade Name
Immunochemistry Systems CAL 2 Calibrator 2
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
15099590232634
Basic UDI
150995901663940MJ
Version Date
April 26, 2024
Manufacturer Last Update
July 21, 2021
Active Status
No
Manufacturer
Manufacturer Name
Beckman Coulter Inc.
Country
United States
Country Type
NON_EU
Address
250 S Kraemer Blvd Brea, CA
Email
BECFA@beckman.com
Authorized Representative
SRN
IE-AR-000000886
Country
Ireland
Address
Lismeehan Clare
Email
ra.clare@beckman.com
Telephone
+353 65 6831100
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
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, Tรผrkiye:None~None, United Kingdom (Northern Ireland only):None~None
Device Characteristics
Human Tissues
Yes
Animal Tissues
No