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Datrend Systems, Inc.

US

Last updated May 30, 2026

What Datrend Systems, Inc. makes

Datrend Systems, Inc. manufactures external defibrillator testers, including devices like the Datrend, PHASE 3 (Model DT-1), and the INFUTEST 2000 Infusion Device Analyzer. These products are designed to evaluate the functionality and performance of external defibrillators and infusion pumps, ensuring compliance and operational readiness.

The company’s portfolio is regulated under Class II medical devices in the US, with devices listed via FDA 510(k) and FDA Unique Device Identification (UDI) registries. The company is based in the United States.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What medical devices does Datrend Systems, Inc. manufacture?

Datrend Systems, Inc. manufactures external defibrillator testers and infusion device analyzers, including models like Datrend, PHASE 3 (Model DT-1), and INFUTEST 2000 Infusion Device Analyzer, which evaluate the functionality of medical equipment.

Where is Datrend Systems, Inc. based?

Datrend Systems, Inc. is based in the United States, as indicated by the country designation in the provided device data.

Which regulatory registries list Datrend Systems, Inc. devices?

Datrend Systems, Inc. devices are listed in the FDA 510(k) and FDA Unique Device Identification (UDI) registries, as specified in the device data.

How are Datrend Systems, Inc. devices classified?

Datrend Systems, Inc. devices are classified as Class II medical devices in the US, meaning they require general controls and special controls to ensure safety and effectiveness.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
US
Address
—
Website
datrend.com
LinkedIn
—
Facebook
—
Phone
604-291-7747
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
249968140

Catalogue (3)

DeviceModel / ReferenceRegistriesClassStatus
Datrend Phase3
FDA UDI
Class IIActive
Phase 3, Model Dt-1 K062099
FDA 510(k)
Class IIActive
Infutest 2000 Infusion Device Analyzer K980165
FDA 510(k)
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

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Authorities

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FDA Establishments (1)

Establishments registered with the FDA under this company group, matched by name.

  • Datrend Systems Inc RICHMOND British Columbia · CA FEI 3002806858