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pursept Xpress FD

EUDAMED

Class IIa (EU MDR)

Ref 70004261

by Schülke & Mayr GmbH

Identity

Trade Name
pursept Xpress  FD EUDAMED
Device Name
mikrozid universal p EUDAMED
Model / Reference
70004261 EUDAMED

Identifiers

Primary DI / UDI-DI
04032651988167 EUDAMED
Basic UDI-DI
4032651BSC00000070AF EUDAMED
EMDN Code
D0799 ALCOHOLS FOR THE DISINFECTION OF MEDICAL DEVICES - OTHER EUDAMED

Classification

Device Class
Class IIa EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

pursept Xpress FD by Schülke & Mayr GmbH — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
DE-MF-000005701

Sources (1)

  • EUDAMED b1aa4451-174f-4847-b71b-6e20b7eaa72c 61 fields · synced Jun 20, 2026