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Pharmpur GmbH

DE-MF-000008337 · Germany · Königsbrunn

Pharmpur GmbH is registered in the European database on medical devices as a manufacturer, with 23 devices declared. It is also registered as a device establishment with the U.S. FDA.

What this manufacturer declares

Class IIb14
Class IIa9

Most frequent device types declared: Packaging variant T2, Packaging variant U2, Packaging variant U1, Packaging variant T1.

Among these devices, 23 are declared sterile, 8 implantable, 1 active.

No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.

United States market access

FDA establishment registerRegistered with FDA
Matched entryPHARMPUR GMBH (DE) · FDA 3005689226
Devices in EUDAMED23
Country of registrationGermany

Notified body certificates

CertificateStatusExpiry
1000276572issued2030-12-10
1000204102issued2030-12-10

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