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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

BABYKEEPER PROBIOTIC 60x120 OPTIMUS — Class I MDR

MD Atlas
Colchones Delax SL

EUDAMED last updated this device on Apr 14, 2026

BABYKEEPER PROBIOTIC 60x120 OPTIMUS

84355822Col_Babykeeper7Q

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Colchones Delax SL
UDI-DI code: 08435582200128
Reference / catalog number: 1234567

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Manufacturer information

Organization name: Colchones Delax SL
SRN: ES-MF-000046525
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 Spain; available across 1 country total.

Country	On market since	Until
SpainPrimary placement	Jan 1, 2019	Still on market

Device identification

Trade name: BABYKEEPER PROBIOTIC 60x120 OPTIMUS
UDI-DI code: 08435582200128
Basic UDI-DI: 84355822Col_Babykeeper7Q
Reference / catalog number: 1234567
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: BABYKEEPER PROBIOTIC 60x120 OPTIMUS
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

V028099NEONATOLOGY AND PEDIATRICS DEVICES - ACCESSORIES NOT INCLUDED IN OTHER CLASSES - 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
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Software identification