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Hydra

EUDAMED

Class I (EU MDR)

Ref LEDBI122-ISCRef LEDBI122

by Lid - Sotramet

Identity

Trade Name
HYDRA EUDAMED
Device Name
HYDRA EUDAMED
Model / Reference
LEDBI122-ISC EUDAMED
LEDBI122 EUDAMED

Identifiers

Primary DI / UDI-DI
03760361830858 EUDAMED
03760361830865 EUDAMED
Basic UDI-DI
376036183HYDRADE EUDAMED
EMDN Code
Z12010702 MOBILE 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

Hydra by Lid - Sotramet — 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
Lid - Sotramet
EUDAMED SRN
FR-MF-000014659

Sources (2)

  • EUDAMED df415dab-90a2-40a9-bea4-4303e41293e8 61 fields · synced Jul 22, 2026
  • EUDAMED 29473c83-0d21-4c46-9246-a9e2edf0c431 61 fields · synced May 18, 2026