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Saebo

EUDAMED

Class I (EU MDR)

Ref K1-MM-100-SD-N-1Model SaeboMASmini

by Saebo Inc.

Identity

Trade Name
Saebo EUDAMED
Device Name
SaeboMASmini EUDAMED
Model / Reference
SaeboMASmini EUDAMED
K1-MM-100-SD-N-1 EUDAMED

Identifiers

Primary DI / UDI-DI
00810018350642 EUDAMED
Basic UDI-DI
081001835SaeboMASminiB7 EUDAMED
EMDN Code
Y241899 ARM, HAND, FINGER FUNCTION AID AND/OR SUBSTITUTION DEVICES - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Austria 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

Saebo by Saebo Inc. — 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
Saebo Inc.
EUDAMED SRN
US-MF-000052039
Authorised Representative
European Healthcare & Device Solutions Ltd. IE-AR-000003999

Sources (1)

  • EUDAMED 63a54298-6862-454c-a598-ecd10aad9d09 61 fields · synced May 22, 2026