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Albert Heijn

EUDAMED

Class IIa (EU MDR)

Ref AH-181850016Model 40-3001/ 780349 / 40-3003 / 780351 / 40-3014 / 752825 / 40-3070 / 2003043 / 40-3071 / 2003041 / 40-3075 / 2003042 / 40-4013 / 752892 / 40-6001 / 781429 / 40-6003 / 781430 / 40-6013 / 781431 / 75-1623 / 781623 / 75-4331 / 754331 / 75-4378 / 754378 Ref AH-181850017

by Aso Llc

Identity

Trade Name
Albert Heijn EUDAMED
Device Name
Non-Sterile Hydrocolloid Bandages EUDAMED
Model / Reference
40-3001/ 780349 / 40-3003 / 780351 / 40-3014 / 752825 / 40-3070 / 2003043 / 40-3071 / 2003041 / 40-3075 / 2003042 / 40-4013 / 752892 / 40-6001 / 781429 / 40-6003 / 781430 / 40-6013 / 781431 / 75-1623 / 781623 / 75-4331 / 754331 / 75-4378 / 754378 EUDAMED
AH-181850016 EUDAMED
AH-181850017 EUDAMED

Identifiers

Primary DI / UDI-DI
08718907348089 EUDAMED
08718907348096 EUDAMED
Basic UDI-DI
0017276M226M3 EUDAMED
EMDN Code
M04040301 HYDROCOLLOID DRESSINGS, NON-COMBINED EUDAMED

Classification

Device Class
Class IIa 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

Albert Heijn by Aso LLC — Class IIa — 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
Aso Llc
EUDAMED SRN
US-MF-000008641
Authorised Representative
Aso Europe BV NL-AR-000004377

Sources (2)

  • EUDAMED d7db437c-9399-405c-b186-9b28f2f77485 61 fields · synced Aug 2, 2026
  • EUDAMED f2b7685f-8a46-479e-9707-41a23f2cfe1f 61 fields · synced May 17, 2026