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Activ8rlives

EUDAMED

Class I (EU MDR)

Ref P111

by Aseptika Limited

Identity

Trade Name
Activ8rlives EUDAMED
Device Name
Activ8rlives4 Health+Wellness App EUDAMED
Model / Reference
P111 EUDAMED

Identifiers

Primary DI / UDI-DI
05060293170946 EUDAMED
Basic UDI-DI
5060293170946UK EUDAMED
EMDN Code
V92 MEDICAL DEVICE SOFTWARE - NOT INCLUDED IN OTHER CLASSES EUDAMED

Classification

Device Class
Class I EUDAMED
Special Device Type
Software EUDAMED
Market of Registration
Northern Ireland 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

Activ8rlives by Aseptika Limited — Class I — 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
Aseptika Limited
EUDAMED SRN
UK-MF-000037607
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 28c95a31-3f43-4ba3-a5b5-ea60542fee0c 61 fields · synced Jun 18, 2026