← Back to catalogue

Rt300-Lsa

EUDAMED

Class IIa (EU MDR)

Ref FA109080Model RT300-LSA

by Restorative Therapies, Inc.

Identity

Device Name
RT300-LSA EUDAMED
Model / Reference
RT300-LSA EUDAMED
FA109080 EUDAMED

Identifiers

Primary DI / UDI-DI
*M720FA10090800U* EUDAMED
Basic UDI-DI
B-*M720FA10090800U* 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

Rt300-Lsa 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

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000023084
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED be548da0-24b0-41fe-bc68-5ee972d4cd53 61 fields · synced Jul 10, 2026