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Sensichlor

EUDAMED

Class I (EU MDR)

Ref 39919Model LATEX GLOVERef 39922Ref 39920

by Bericah S.p.A.

Identity

Trade Name
SENSICHLOR EUDAMED
Device Name
GUANTO MONOUSO IN LATTICE SENZA POLVERE NON STERILE EUDAMED
Model / Reference
LATEX GLOVE EUDAMED
39919 EUDAMED
39922 EUDAMED
39920 EUDAMED

Identifiers

Primary DI / UDI-DI
08024151399198 EUDAMED
08024151399228 EUDAMED
08024151399204 EUDAMED
Basic UDI-DI
8024151GULSYS EUDAMED
Direct Marketing DI
08024151399198 EUDAMED
08024151399228 EUDAMED
08024151399204 EUDAMED
EMDN Code
T010201 LATEX EXAMINATION / TREATMENT GLOVES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

Yes

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

Yes

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Sensichlor by Bericah S.p.A. — 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
Bericah S.p.A.
EUDAMED SRN
IT-MF-000007397

Sources (3)

  • EUDAMED bcb92bcb-3006-4a9c-a566-dbc60175ea27 61 fields · synced Jul 31, 2026
  • EUDAMED 0b2986cf-f122-4627-b563-1ccf3e000500 61 fields · synced May 17, 2026
  • EUDAMED fe67752d-a1ee-4e92-bcdb-b4f860685f21 61 fields · synced May 18, 2026