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Pharma Systems AB

Also registered as Pharma System AB, Pharma Systems, Inc.

Country not established

Pharma Systems AB is a medical device manufacturer, with 157 devices listed in EUDAMED and FDA 510(k) (EU Class IIa; FDA Class I and II) as of 15 Nov 2026.

Devices
157

Registry facts

Counted by deviCERTS from registry records, 15 Nov 2026

Registries
  • EUDAMED 150
  • FDA 510(k) 7

A device listed in two registries counts in both.

Device classes
  • EU Class IIa 150
  • FDA Class I 4
  • FDA Class II 3
Sites and related companies

What Pharma Systems AB makes

Pharma Systems AB manufactures the BACT-TRAP HEPA MIDI, a Class II medical device designed to filter airborne contaminants, including bacteria, in controlled environments such as pharmaceutical manufacturing or cleanroom settings.

The device is regulated under the FDA’s 510(k) pathway as a Class II product and is listed in the FDA’s 510(k) database.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue157

Newest first, rows 1-50 of 157

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Rows 1-50 of 157

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Sites1

Frequently asked questions

How many devices does Pharma Systems AB have in the registry?

The registry currently lists 157 devices for Pharma Systems AB. Devices recorded under merged duplicate company entries are counted once.

Which registries list Pharma Systems AB's devices?

Among its 50 most recently registered devices, Pharma Systems AB has devices listed in EUDAMED (50 devices).

What risk classes do Pharma Systems AB's devices fall under?

Among its 50 most recently registered devices, the classes recorded for Pharma Systems AB's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from Pharma Systems AB in the registry?

The most recently registered devices listed for Pharma Systems AB include Bact HME Midi Port and PharmaFlex Swivel Port, Pharma Trach Oxygen Supply, Bact HME Port and Elbow and Pharma Mini Port Angle.

Generated automatically from registry data and not verified by a human reviewer.