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Eqtfhs010 Sat16

EUDAMED

Class I (EU MDR)

Ref ARDSAT239023A

by Maquet SAS

Identity

Trade Name
EQTFHS010 SAT16 EUDAMED
Device Name
Maquet Equipment EUDAMED
Model / Reference
ARDSAT239023A EUDAMED

Identifiers

Primary DI / UDI-DI
03700712420208 EUDAMED
Basic UDI-DI
3700712421267RG EUDAMED
Direct Marketing DI
03700712420208 EUDAMED
EMDN Code
Z12010799 SCIALYTIC LAMP LIGHTING SYSTEMS - OTHER 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

Eqtfhs010 Sat16 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 0ad6f696-7040-4b3e-980a-b55e61f68693 61 fields · synced Jul 27, 2026