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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

Testdevice — Class IIa MDD by Feuerstein GmbH

MD Atlas
Feuerstein GmbH

EUDAMED last updated this device on Mar 23, 2026

Testdevice

B-04255574519311

On the marketClass IIa

Applicable legislation: MDD [Directive 93/42/EEC on medical devices]
Organization name: Feuerstein GmbH
UDI-DI code: 04255574519311
Reference / catalog number: Testdevice

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Manufacturer information

Organization name: Feuerstein GmbH
SRN: DE-MF-000006770
Manufacturer status: Active

Market distribution

Primary placement in Germany; available across 1 country total.

Country	On market since	Until
GermanyPrimary placement	Jan 1, 2005	Still on market

Device identification

Trade name: not provided
UDI-DI code: 04255574519311
Basic UDI-DI: B-04255574519311
Reference / catalog number: Testdevice
Issuing entity: GS1

Classification

Risk category: Class IIa
Applicable legislation: MDD [Directive 93/42/EEC 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)

L0202SUTURE NEEDLES, REUSABLE

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

14380425557453000BQOn the market G503000425557451000BAOn the market G503000S425557452000BHOn 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.