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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

150018 — Class IIb MDR by Dr. Kleine Pharma GmbH

MD Atlas
Dr. Kleine Pharma GmbH

EUDAMED last updated this device on Aug 26, 2025

150018

40395374446N

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Dr. Kleine Pharma GmbH
UDI-DI code: 04064761001917
Reference / catalog number: 150018

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Manufacturer information

Organization name: Dr. Kleine Pharma GmbH
SRN: DE-MF-000006589
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Dec 18, 2025	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04064761001917
Basic UDI-DI: 40395374446N
Reference / catalog number: 150018
Issuing entity: GS1

Classification

Risk category: Class IIb
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Status: On the market

Device details

Quantity: 1
Additional product description: —
Additional information URL: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

G99GASTROINTESTINAL 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

44440395374446NOn the market 44440395374446NOn the market 39134540395374446NOn the market 457B-4577MOn the market 060B-0606NOn 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.