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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

002283050 — Class I MDR by RfQ-Medizintechnik GmbH…

MD Atlas
RfQ-Medizintechnik GmbH & Co. KG

EUDAMED last updated this device on Mar 18, 2026

002283050

426074483095AT

On the marketClass I

Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Organization name: RfQ-Medizintechnik GmbH & Co. KG
UDI-DI code: 04260744834538
Reference / catalog number: 002283050

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Manufacturer information

Organization name: RfQ-Medizintechnik GmbH & Co. KG
SRN: DE-MF-000007646
Manufacturer status: Active

Related devices

002293040426074483095ATOn the market v426074483095ATOn the market 002111041426074483095ATOn the market 002111025426074483095ATOn the market 002111050426074483095ATOn the market

Critical warnings

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

CW011
EUDAMED did not publish a description for this code.
CW010
EUDAMED did not publish a description for this code.

Market distribution

Primary placement in Germany; available across 1 country total.

Placed on the market in Germany; per-country availability dates not published.

Device identification

Trade name: not provided
UDI-DI code: 04260744834538
Basic UDI-DI: 426074483095AT
Reference / catalog number: 002283050
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: No additional information URL provided by the manufacturer.
Clinical sizes: No clinical sizes registered for this device.

EMDN nomenclature code(s)

Z12029080VARIOUS INSTRUMENTS FOR ENDOSCOPY AND MINI-INVASIVE SURGERY - HARDWARE ACCESSORIES

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.