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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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Organization name
UDI-DI code
Reference / catalog number

Nexcare™ Bandages finger plaster… — Class I MDR

MD Atlas
3M Deutschland GmbH (Medical)

EUDAMED last updated this device on May 20, 2026

Nexcare™ Bandages finger plaster flexible comfort

06082232761050000000010GA

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: 3M Deutschland GmbH (Medical)
UDI-DI code: 04054596758940
Reference / catalog number: NFP001W

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Manufacturer information

Organization name: 3M Deutschland GmbH (Medical)
SRN: DE-MF-000011641
Manufacturer status: Active

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Certificates

No certificates registered for this manufacturer.

No certificate references this Basic UDI-DI, because: • It does not require a certificate, or • It only requires a certificate without a Basic UDI-DI reference (e.g. a QMS certificate), or • The required certificate(s) referencing this Basic UDI-DI have not been registered yet.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: Nexcare™ Bandages finger plaster flexible comfort
UDI-DI code: 04054596758940
Basic UDI-DI: 06082232761050000000010GA
Reference / catalog number: NFP001W
Issuing entity: GS1

Classification

Risk category: Class I
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 10
Additional product description: —
Additional information URL: https://www.3m.com/3M/en_WW/ifu-select-location/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

M04010102POLYURETHANE (OR OTHER MATERIAL) ADHESIVE DRESSINGS, WITH ABSORBENT PAD

Compliance flags

Safety

Sterile

Single use

Contains latex

Reprocessed single-use

Direct marking

Substances

CMR substance

Endocrine disruptor

Regulatory

Annex XVI applicable

Sterilization

Lifecycle

New device

UDI-PI traceability

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Expiration date
Manufacturing date
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Software identification