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Rilifine

EUDAMED

Class I (EU MDR)

Ref N/AModel ⅢA

by Tianjin Rilifine Medical Device Co., Ltd

Identity

Trade Name
RILIFINE EUDAMED
Device Name
Lancing Device EUDAMED
Model / Reference
ⅢA EUDAMED
N/A EUDAMED

Identifiers

Primary DI / UDI-DI
16975522993004 EUDAMED
Basic UDI-DI
697552299LDA300K7 EUDAMED
EMDN Code
A018099 NEEDLES - OTHER ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Category: Electromagnetic surgical navigation device tracking system

Rilifine by Tianjin Rilifine Medical Device Co., Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Electromagnetic surgical navigation device tracking system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
CN-MF-000026981
Authorised Representative
Sungo Cert GmbH DE-AR-000010869

Sources (1)

  • EUDAMED 23f4c5c0-0d6a-4698-af52-37b018af2cfe 61 fields · synced Jun 19, 2026