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Alissa Interpret - EUDAMED Registration 05700574035631

Access comprehensive regulatory information for Alissa Interpret 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 05700574035631 and manufactured by Agilent Technologies Singapore (International) Pte Ltd in Singapore.

This page provides complete registration details including trade name (Alissa Interpret), manufacturer information, authorized representative details, competent authority (Danish Medicines Agency, Pharmacovigilance & Medical Devices), 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
05700574035631
No
Alissa Interpret
Trade Name: Alissa Interpret
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Device Description (EMDN)

VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE

Device Classification
Risk Class
Class A
CND Nomenclatures Code
W02079092
Trade Name
Alissa Interpret
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
05700574035631
Basic UDI
570057R0403P3011A040300MM
Version Date
June 28, 2024
Manufacturer Last Update
October 15, 2021
Active Status
No
Manufacturer
Country
Singapore
Country Type
NON_EU
Address
1 Yishun Avenue 7 Singapore
Email
info.dk@agilent.com
Authorized Representative
SRN
DK-AR-000001443
Country
Denmark
Address
42 Produktionsvej Glostrup
Email
info.dk@agilent.com
Telephone
+45 44 85 95 00
Regulatory Information
Competent Authority
Danish Medicines Agency, Pharmacovigilance & Medical Devices
Applicable Legislation
IVDR (REGULATION (EU) 2017/746 on in vitro diagnostic medical devices)
Placed On The Market
Denmark
Device Characteristics
Human Tissues
No
Animal Tissues
No