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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

Clipp — Class I MDR by BIOMIMETIK

MD Atlas
BIOMIMETIK

EUDAMED last updated this device on May 10, 2026

Clipp

3770027591ClippGN

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: BIOMIMETIK
UDI-DI code: 03770027591016
Reference / catalog number: SKU0002-KPU

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Manufacturer information

Organization name: BIOMIMETIK
SRN: FR-MF-000032672
Manufacturer status: Active

Critical warnings

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

CW011
utiliser sous surveillance d'un adulte. Lire attentivement la notice avant utilisation

Market distribution

Primary placement in France; available across 1 country total.

Country	On market since	Until
FrancePrimary placement	Sep 1, 2022	Still on market

Device identification

Trade name: Clipp
UDI-DI code: 03770027591016
Basic UDI-DI: 3770027591ClippGN
Reference / catalog number: SKU0002-KPU
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: Dispositif de sevrage de la succion chez l'enfant
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Q0199ODONTOLOGY DEVICES - 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

Related devices

Clipp3770027591ClippGNOn the market Clipp3770027591ClippGNOn the market

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.