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Humidity Chamber

EUDAMED

Class A (EU MDR)

Ref 1270

by sebia

Identity

Trade Name
HUMIDITY CHAMBER EUDAMED
Device Name
HUMIDITY CHAMBER EUDAMED
Model / Reference
1270 EUDAMED

Identifiers

Primary DI / UDI-DI
03607360012703 EUDAMED
Basic UDI-DI
3607361270BUC4 EUDAMED
EMDN Code
W020105019099 VARIOUS ELECTROPHORESIS INSTRUMENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Humidity Chamber by Sebia — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
sebia
EUDAMED SRN
FR-MF-000003520

Sources (1)

  • EUDAMED ad76acc2-04db-49ef-94a5-c7cb24e4a25b 61 fields · synced Jun 17, 2026