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emVia Lancing Device

EUDAMED

Class I (EU MDR)

Ref -

by i-SENS, Inc.

Identity

Trade Name
emVia Lancing Device EUDAMED
Device Name
Lancing Device EUDAMED
Model / Reference
- EUDAMED

Identifiers

Primary DI / UDI-DI
08806712005003 EUDAMED
Basic UDI-DI
8806712LC001SF EUDAMED
EMDN Code
V9099 VARIOUS DEVICES NOT INCLUDED IN OTHER CLASSES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Germany 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: Device sterilization/disinfection container, reusable

emVia Lancing Device by i-SENS, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Device sterilization/disinfection container, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
i-SENS, Inc.
EUDAMED SRN
KR-MF-000009173
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 00c5fa7f-741e-4757-a69f-1d0f4c8fcaa0 61 fields · synced Jun 18, 2026