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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

CD2612NL — Class I MDR by Millet Innovation

MD Atlas
Millet Innovation

EUDAMED last updated this device on Apr 23, 2026

CD2612NL

366039600004AB

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Millet Innovation
UDI-DI code: 03660396009338
Reference / catalog number: CD2612NL

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Manufacturer information

Organization name: Millet Innovation
SRN: FR-MF-000004611
Manufacturer status: Active

Related devices

CD2612PT366039600004ABOn the market CD2611PT366039600004ABOn the market CD2613PT366039600004ABOn the market CC2612PT366039600001A5On the market CC2614PT366039600001A5On the market

Critical warnings

4 warnings recorded — scroll inside the panel to see all entries.

CW011
Do not use on skin lesions.
CW030
In the case of people with arteritis, diabetes, polyneuritis, neuropathy of the lower limbs or ulcers: ask your doctor or podiatrist for advice, then monitor your foot during use.
CW010
EUDAMED did not publish a description for this code.
CW262
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Netherlands; available across 1 country total.

Country	On market since	Until
NetherlandsPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 03660396009338
Basic UDI-DI: 366039600004AB
Reference / catalog number: CD2612NL
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: 1
Additional product description: Coussinets Double protection-M-
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: 39–41 MU162

EMDN nomenclature code(s)

Y99DEVICES FOR PERSONS WITH DISABILITIES NOT INCLUDED IN OTHER CATEGORIES - OTHER

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

Batch number
Expiration date
Manufacturing date
Serial number
Software identification

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.