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Sf750

EUDAMED

Class IIb (EU MDR)

Ref SF750

by Memmert GmbH + Co.KG

Identity

Device Name
SF750 EUDAMED
Model / Reference
SF750 EUDAMED

Identifiers

Primary DI / UDI-DI
04251817501686 EUDAMED
Basic UDI-DI
B-04251817501686 EUDAMED
EMDN Code
S9099 STERILISATION DEVICES (EXCLUDING CAT. D - Z) - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sf750 by Memmert GmbH + Co.KG — Class IIb — MDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

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Manufacturer

EUDAMED SRN
DE-MF-000012127

Sources (1)

  • EUDAMED 9845af2f-70cc-4c14-a105-a2f1ac682ab2 61 fields · synced Jun 19, 2026