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Doigtier

EUDAMED

Class I (EU MDR)

Ref A1052

by Medistock

Identity

Trade Name
DOIGTIER EUDAMED
Device Name
DOIGTIER EUDAMED
Model / Reference
A1052 EUDAMED

Identifiers

Primary DI / UDI-DI
03700425939172 EUDAMED
Basic UDI-DI
03700425NS-classI-002W3 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

Doigtier 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 24adc744-3eff-4a1a-b61f-a10771b41b68 61 fields · synced Jul 17, 2026