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OneTouch Vita™ Receiver

EUDAMED

Class IIb (EU MDR)

Ref CGM-R-004

by i-SENS, Inc.

Identity

Trade Name
OneTouch Vita™ Receiver EUDAMED
Device Name
Receiver EUDAMED
Model / Reference
CGM-R-004 EUDAMED

Identifiers

Primary DI / UDI-DI
08806712011349 EUDAMED
Basic UDI-DI
8806712CGMR001T5 EUDAMED
EMDN Code
Z1204011599 BLOOD SUGAR MONITORING SYSTEMS - 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

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

Yes

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

OneTouch Vita™ Receiver by i-SENS, Inc. — Class IIb — MDR — listed in EUDAMED — regulatory data on deviCERTS

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 a903de45-f805-4932-b19f-050ea9d72808 61 fields · synced Jun 19, 2026