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ALLYpro

EUDAMED

Class IIb (EU MDR)

Ref HS-FE-51

by i-SENS, Inc.

Identity

Trade Name
ALLYpro EUDAMED
Device Name
Glucose Data Management Software EUDAMED
Model / Reference
HS-FE-51 EUDAMED

Identifiers

Primary DI / UDI-DI
08806712009612 EUDAMED
Basic UDI-DI
8806712CGMDM001UV EUDAMED
EMDN Code
Z1204011599 BLOOD SUGAR MONITORING SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class IIb EUDAMED
Special Device Type
Software 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

ALLYpro 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 c4bc6c6f-aac4-49eb-9138-18d36be87c42 61 fields · synced Jul 24, 2026