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Ezea33df Tk Sb1011

EUDAMED

Class I (EU MDR)

Ref ARDEZA209012A

by Maquet SAS

Identity

Trade Name
EZEA33DF TK SB1011 EUDAMED
Device Name
Maquet Ezea EUDAMED
Model / Reference
ARDEZA209012A EUDAMED

Identifiers

Primary DI / UDI-DI
03700712435868 EUDAMED
Basic UDI-DI
3700712432942SM EUDAMED
Direct Marketing DI
03700712435868 EUDAMED
EMDN Code
Z12010701 FIXED SCIALYTIC LAMPS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France 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

Ezea33df Tk Sb1011 by Maquet Sas — 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
Maquet SAS
EUDAMED SRN
FR-MF-000002926

Sources (1)

  • EUDAMED 846ff301-ba8c-48d2-8f2e-ee85c9886e6e 61 fields · synced Aug 1, 2026