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myMedi LATEX PLUS

EUDAMED

Class I (EU MDR)

Ref A1406MP

by Medistock

Identity

Trade Name
myMedi LATEX PLUS EUDAMED
Device Name
GANT EUDAMED
Model / Reference
A1406MP EUDAMED

Identifiers

Primary DI / UDI-DI
03700425953604 EUDAMED
Basic UDI-DI
03700425NS-classI-001VZ EUDAMED
EMDN Code
T010201 LATEX EXAMINATION / TREATMENT GLOVES 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

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

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

myMedi LATEX PLUS by Medistock — 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
Medistock
EUDAMED SRN
FR-MF-000007667

Sources (1)

  • EUDAMED 47747906-10f3-4794-898c-a5f75ba31aa7 61 fields · synced Sep 17, 2026