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Spectra+ Soft Case

EUDAMED

Class I (EU MDR)

Ref 3412-P-7002

by Keeler Ltd

Identity

Trade Name
SPECTRA+ SOFT CASE EUDAMED
Device Name
LIO CARRY CASE & CARTON EUDAMED
Model / Reference
3412-P-7002 EUDAMED

Identifiers

Primary DI / UDI-DI
05055272708463 EUDAMED
Basic UDI-DI
50552727CASESFD EUDAMED
EMDN Code
Z12120180 OPHTALMOLOGY ASSESSMENTS AND DIAGNOSIS INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Finland 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

Spectra+ Soft Case by Keeler Ltd — 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
Keeler Ltd
EUDAMED SRN
GB-MF-000009031
Authorised Representative
Keeler Europe Distribution, S.L. ES-AR-000001559

Sources (1)

  • EUDAMED df0abed6-7406-4e1e-8fc6-0bf7629244a2 61 fields · synced Aug 1, 2026