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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

511000500 — Class I MDR by Injex Pharma GmbH

MD Atlas
Injex Pharma GmbH

EUDAMED last updated this device on Apr 22, 2026

511000500

426239401511000500YZ

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: Injex Pharma GmbH
UDI-DI code: 04262394010058
Reference / catalog number: 511000500

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Manufacturer information

Organization name: Injex Pharma GmbH
SRN: DE-MF-000006766
Manufacturer status: Active

Critical warnings

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

CW009
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	Jul 1, 2026	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04262394010058
Basic UDI-DI: 426239401511000500YZ
Reference / catalog number: 511000500
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: —
Additional information URL: https://www.injex.de/
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

A070103INFUSION TUBING ADAPTERS AND CONNECTORS

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

5460004004262394015460004005DOn the market 511000700426239401511000700ZBOn the market 3380110014262394013380110014EOn the market 3380130004262394013380130004SOn the market 511000800426239401511000800ZGOn 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.