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Manufacturer profile

Agilent Technologies, Inc.

EU EUDAMEDUnited States47 registered devices
VerifiedEUDAMED · official EU database
47
Total devices
2
Risk classes
2022
Earliest version
2024
Latest version
Regulatory footprint
Search Agilent Technologies, Inc. across other regulatory registries
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Recent products (latest 10)
Most recently updated devices in the database
GenetiSure Dx Universal aCGH Reagents
05700571112618
Class A
GenetiSure Dx Universal aCGH Reagents
05700571112632
Class A
GenetiSure Dx Universal aCGH Reagents
05700571112656
Class A
GenetiSure Dx Universal aCGH Reagents
05700571112625
Class A
GenetiSure Dx Universal aCGH Reagents
05700571112649
Class A
GenetiSure Dx Universal aCGH Reagents
05700571112601
Class A
GenetiSure Dx Postnatal Assay
05700571108697
Class C
Agilent CytoDx Software
05700574037437
Class C
Epoch
05700574035020
Class A
800TS
05700574036911
Class A
Risk class distribution
Breakdown by risk classification
Class A4595.7% of total
Class C24.3% of total
Top authorized representatives
Most common authorized representatives for this manufacturer
Agilent Technologies Denmark ApS
100.0%47 devices
About this profile

Explore comprehensive manufacturer profile for Agilent Technologies, Inc. through Pure Global AI's free EU medical device database. This company manufactures 47 medical devices registered with EUDAMED across 2 risk classes based in United States.

This page provides detailed insights including recent registrations, risk class distribution (Class A: 45, Class C: 2), and complete regulatory information from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry.