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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

BÉABA MINIDOO — Class I MDR by Rokána Kft.

MD Atlas
Rokána Kft.

EUDAMED last updated this device on Mar 12, 2026

BÉABA MINIDOO

59981771000000000000001DX

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Rokána Kft.
UDI-DI code: 05998177100027
Reference / catalog number: 002

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Manufacturer information

Organization name: Rokána Kft.
SRN: HU-MF-000048032
Manufacturer status: Active

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: BÉABA MINIDOO
UDI-DI code: 05998177100027
Basic UDI-DI: 59981771000000000000001DX
Reference / catalog number: 002
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: Mouche-bébé par aspiration
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12159009EQUIPMENT FOR REMOVAL OF SECRETIONS

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

BIOSYNEX59981771000000000000001DXOn the market 00459981771000000000000001DXOn the market TOMYKA MINIDOO59981771000000000000001DXOn 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.