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EUDAMED registration 05700574037314No

BenchLab CNV Software

Agilent Technologies Singapore (International) Pte LtdClass AEU EUDAMEDTrade name: BenchLab CNV Software
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class A
CND nomenclatures code
W02079092
Trade name
BenchLab CNV Software
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
05700574037314
Basic UDI
570057R0403P3011A040800NE
Version date
February 25, 2025
Manufacturer last update
October 15, 2021
Active status
No
Manufacturer
Manufacturer name
Agilent Technologies Singapore (International) Pte Ltd
Country
Singapore
Country type
NON_EU
Address
1 Yishun Avenue 7 Singapore
Email
info.dk@agilent.com
Authorized representative
Name
Agilent Technologies Denmark ApS
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
Device description (EMDN)

VARIOUS GENERAL PURPOSE IVD INSTRUMENTS - IVD MEDICAL DEVICE SOFTWARE

About this record

Access comprehensive regulatory information for BenchLab CNV Software 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 05700574037314 and manufactured by Agilent Technologies Singapore (International) Pte Ltd in Singapore.

This page provides complete registration details including trade name (BenchLab CNV Software), 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.