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Da

EUDAMED

Class I (EU MDR)

Ref VH-OT-0101-1Model 39-0441 / 39-0447 / 39-0449 / 39-0459 / 39-0465 / 39-0467 / 39-0469 / 39-0480 / 39-0483 / 39-0491 / 39-0511 / 39-0624 / 39-0626 / 39-0633 / 39-0658 / 39-0925 / 39-1459

by Aso Philippines, Inc.

Identity

Trade Name
DA EUDAMED
Device Name
Fabric (Dark and Light) adhesive bandages EUDAMED
Model / Reference
39-0441 / 39-0447 / 39-0449 / 39-0459 / 39-0465 / 39-0467 / 39-0469 / 39-0480 / 39-0483 / 39-0491 / 39-0511 / 39-0624 / 39-0626 / 39-0633 / 39-0658 / 39-0925 / 39-1459 EUDAMED
VH-OT-0101-1 EUDAMED

Identifiers

Primary DI / UDI-DI
08715886021101 EUDAMED
Basic UDI-DI
48079990API057NC EUDAMED
EMDN Code
M0599 MEDICAL PLASTERS - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands 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

A comprehensive overview of the DA device, including its purpose, features, and regulatory compliance.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
PH-MF-000027714
Authorised Representative
Aso Europe BV NL-AR-000004377

Sources (1)

  • EUDAMED 514f1c0f-ef46-4587-92a4-6143068706b5 61 fields · synced Jul 24, 2026