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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

KAWAI FRIENDS BAND AIDS BOX SM DL12 — Class I MDR

MD Atlas
POLYFLAME EUROPE SAS

EUDAMED last updated this device on Mar 10, 2026

KAWAI FRIENDS BAND AIDS BOX SM DL12

3661075JDAB009F3

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: POLYFLAME EUROPE SAS
UDI-DI code: 03661075030308
Reference / catalog number: 40 509 098

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Manufacturer information

Organization name: POLYFLAME EUROPE SAS
SRN: FR-MF-000042860
Manufacturer status: Active

Critical warnings

1 warning recorded — scroll inside the panel to see all entries.

CW011
WARNINGS. Do not use if package is damaged. Clean, disinfect, rinse and dry the wound and its surroundings carefully. Apply the dressing by smoothing the edges. Change the dressing at least twice a day.

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Market distribution

Primary placement in France; available across 1 country total.

Placed on the market in France; per-country availability dates not published.

Device identification

Trade name: KAWAI FRIENDS BAND AIDS BOX SM DL12
UDI-DI code: 03661075030308
Basic UDI-DI: 3661075JDAB009F3
Reference / catalog number: 40 509 098
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: 24
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

UDI-PI traceability

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

EMDN nomenclature code(s)

European Medical Device Nomenclature — the EU product classification assigned to this device.

M03030202SKIN PROTECTIVE BANDAGES

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

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3661075KCR24053FQ

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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.