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Xl Care Dermic Film

EUDAMED

Class I (EU MDR)

Ref 039373-02-00

by Adhex Technologies Sas

Identity

Device Name
XL CARE DERMIC FILM EUDAMED
Model / Reference
039373-02-00 EUDAMED

Identifiers

Primary DI / UDI-DI
03760339170917 EUDAMED
Basic UDI-DI
376033917DermicFilmHS EUDAMED
Unit of Use DI
03760339170900 EUDAMED
EMDN Code
M04010102 POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD 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

Xl Care Dermic Film by Adhex Technologies Sas — 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

EUDAMED SRN
FR-MF-000009493

Sources (1)

  • EUDAMED e50a223c-530f-4356-a45a-5e71cd173494 61 fields · synced Jun 18, 2026