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Organization name
UDI-DI code
Reference / catalog number

04260753841619 — Class IIb MDR by Fairpharm Vertriebs GmbH

MD Atlas
Fairpharm Vertriebs GmbH

EUDAMED last updated this device on Jan 27, 2026

04260753841619

426075384E1115D01MZ

On the marketClass IIb

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Fairpharm Vertriebs GmbH
UDI-DI code: 04260753841619
Reference / catalog number: 04260753841619

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Manufacturer information

Organization name: Fairpharm Vertriebs GmbH
SRN: DE-MF-000016959
Manufacturer status: Active

Related devices

04260753841510426075384E0730C01PCOn the market 04260753841992426075384E0730C01PCOn the market 04260753841657426075384E0730C01PCOn the market 04260753841596426075384E0730C01PCOn the market 04260753841572426075384E0730C01PCOn the market

Critical warnings

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

CW275
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.
CW032
EUDAMED did not publish a description for this code.
CW277
EUDAMED did not publish a description for this code.
CW135
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement		Still on market

Device identification

Trade name: not provided
UDI-DI code: 04260753841619
Basic UDI-DI: 426075384E1115D01MZ
Reference / catalog number: 04260753841619
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: 10
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)

G0401ORALLY ADMINISTERED DEVICES FOR THE THERAPY OF GASTRO-INTESTINAL DISORDERS

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.