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UE FES Existing Rt300-SL

EUDAMED

Class IIa (EU MDR)

Ref SA105419

by Restorative Therapies, Inc.

Identity

Device Name
UE FES Existing Rt300-SL EUDAMED
Model / Reference
SA105419 EUDAMED

Identifiers

Primary DI / UDI-DI
*M720SA1054190U* EUDAMED
Basic UDI-DI
B-*M720SA1054190U* EUDAMED
EMDN Code
Y99 DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - OTHER EUDAMED

Classification

Device Class
Class IIa 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

UE FES Existing Rt300-SL by Restorative Therapies, Inc. — Class IIa — 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
US-MF-000023084
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED c7ff1a1f-60c1-48b8-a4b7-c188b0d0cbcd 61 fields · synced Jun 18, 2026